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#iso 9001 bas denetim sorulari#iso 9001 uygunsuzluk listesi#iso 9001 audit checklist#iso 9001 major minor#kalite yonetim kontrol listesi#iso 9001 denetim sorulari 2024#iso 9001 quality audit#iso 9001 denetim raporu#iso 9001 sertifikasyon#iso 9001 ic denetim#iso 9001 uygunsuzluk tespiti#kalite yonetim sistemi egitimi#iso 9001 uygunsuzluk raporu#iso 9001 sertifika denetimi#kalite denetim sorulari#iso 9001 denetim standartlari#iso 9001 belgesi nasil alinir#iso 9001 denetci kontrol listesi#iso 9001 denetim kriterleri#iso 9001 ic denetim proseduru#iso 9001 belgelendirme denetimi#iso 9001 performans denetimi#iso 9001 surec denetimi#iso 9001 denetim adimlari#iso 9001 surec yonetimi
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Basins Suppliers
Basins suppliers are essential for preventing river, lake and water table pollution. They prevent solid materials from clogging drainage systems and allowing them to pass into bodies of water. They also filter out large particles.
The best basins are made from high-quality materials that are durable and look great in your washroom. They should last you a long time, and you should be able to find one that matches your bathroom’s design.
Suppliers of plastic basins
Plastic basins are ideal for a wide range of everyday tasks. They’re durable, sturdy, and easy to clean. They’re also versatile and save space in the kitchen. You can use them to wash dishes, soaking laundry, or for hand-washing fruits and vegetables. They’re also great for storing supplies, and can help you clean up after a party.
Manufacturer of rectangular and cylindrical secondary containment basins for reducing liquid & debris spills. Products meet EPA & Uniform Fire Code Spill Containment Regulations. Serves the automotive, fire protection/sprinkler system, food processing, marine, mining, paper, petroleum, textile, transportation, and water industries. JIT delivery available.
Custom fabricator of molded and extruded polymer products. Capabilities include bending, engineering, field fabrications, machining, welding, and designing. Products include ductwork, enclosures, cabinets, fume hoods, gratings, liners, manifolds, and tanks. Also offers field repairs and 24 hour emergency service. ISO 9001:2015 certified. Based in USA.
Suppliers of fiberglass reinforced plastic basins
FRP basins are made from fiberglass or a similar material and provide the advantage of being resistant to corrosion, lightweight for easy handling, and low electrical conductivity. They are suitable for a wide variety of applications. They are also non-absorbent and resistant to chemicals. These benefits make them a great choice for industrial and manufacturing applications.
FRP Fabricators of standard & custom containers, tanks & baskets. Capabilities include hand lay up open & spray up molding, cold press forming, RTM Lite & Vacuum Bagging, CNC precision trimming & engineering prints. Serves industrial, marine, food & beverage industries.
Minority owned custom fabricator of corrosion resistant fiberglass & plastic products. Capabilities include open & closed mold composite fiberglass fabrication, light metal fabrication & product assembly for major original equipment manufacturers. Products are sold worldwide. Offers a full range of design, engineering, fabrication & field service. Meets EPA, UNFCCC & NFPA standards. Other products include chemists' basins, modular rooms & VSE balance enclosures for industrial, chemical, pharmaceutical & biotech, schools & universities, government & medical applications.
Suppliers of concrete catch basins
A catch basin is a concrete box that sits underground and is the primary component of many drainage systems. It has a grate and is filled with drainage pipe. During rainy weather, this drainage system prevents lawns and homes from flooding. In addition, it helps reduce insect infestation and mildew. It also improves resale value.
In order to work properly, the catch basin must be cleaned and examined regularly. Fortunately, there are companies that specialize in this task. These professionals will examine the grates of catch basins and remove any dirt that has accumulated. It is important to clean and examine these grates as they are a source of contamination.
The purpose of the catch basin is to catch sediment and large debris that may be found in rainwater. It prevents these materials from entering sewer or storm drain pipes and clogging them. The sump of the catch basin is designed to trap these items and divert them into an outlet location (ditch, creek, river, lake, ocean). This process reduces pollutants such as floatables, trash, free oils, and sediment.
Suppliers of plastic or polymer concrete catch basins
Many excavating contractors think of large precast concrete catch basins when they discuss drainage systems. These structures are often used at the entry point to runoff or standing water drainage systems in municipal, state and federal drainage projects. They prevent small-scale drainage systems from becoming clogged, which can decrease their effectiveness. They are also widely used in landscape drainage applications.
There are several different types of plastic and polymer concrete catch basins available for commercial, industrial, and residential use. These basins are often designed for a variety of pipe sizes, and can be customized with different frames and grates. They also feature a range of accessories, including drain risers and covers.
If you're in need of a new catch basin, check out Foster Supply's Weholite line. This product is a great solution for failing drainage structures that are too costly to replace with standard replacement techniques. It also allows existing pipes to be lined in place without digging up the entire pipe and surrounding area.
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Confused about the difference between minor & major non-conformances in the ISO 9001 Quality Management System? Understand them for the betterment of your firm.
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What are the different types of ISO Certification in Ghana?
Introduction:
ISO Certification in Ghana, Factocert is a professional multi-skilled leading ISO Consultants in Ghana which has Provided ISO 9001:2008 Certification Services in Accra, Kumasi, Tema, Tamale, Cape Coast, Accra, Accra and other major cities in Ghana with Implementation, Documentation, Audit, Templates, Training, Gap Analysis, Registration at an affordable cost to all organizations seeking certification under the Quality Management System in Ghana.
Delivering high-quality goods & services is important to assist in the market. With ISO Consultants in Ghana, your Organization will be able to improve its credibility and overall efficiency. An ISO specification refers to an organization that sets international standards. The ISO is an independent organization that sets standards for the safety, efficiency and quality of services and products provided by the Organization, given light of the increasing competition among Organizations.
Process of getting ISO Certification in Ghana
Pre-requisite to ISO Certification Process in Ghana
Process for ISO Certification in Ghana
Costs associated with ISO certification.
Acquiring ISO certification in Ghana requires a pre-requisite
Choosing the type of ISO Certification in Ghana
You must first decide what type of ISO certification your Organization needs.
Various types of ISO certification are available, including:
Quality Management System – ISO 9001, ISO 9001 certification in Ghana
Food safety management system – ISO 22000, ISO 22000 certification in Ghana
Information Security Management System – ISO 27001, ISO 27001 certification in Ghana
Environmental Management System – ISO 14001, ISO 14001certification in Ghana
Choosing an ISO Certification Body in Ghana
You must choose a recognized and credible ISO certification body in Ghana.
While picking the ISO registration in Ghana. It is important to keep in mind the following:
Make sure you check out several ISO Certification service providers in Ghana.
Process for ISO Certification in Ghana
Firstly, Make an application
The client and the registrar should agree on commitment. In addition to liability issues, confidentiality, and access rights, this commitment determines the rights and obligations of both parties.
Review of quality documents
Our ISO Consultants in Ghana will review all of your quality manuals & documents related to various policies & procedures that are being followed in your organization. ISO auditors can identify weaknesses in the ISO standards by recalling existing work.
Create a plan of action.
If the ISO auditor identifies gaps in your organization, you should arrange an action plan to close them. You must prepare a list of the mandatory tasks to bring the chosen changes to your organization. You may be forced to train your employees to work efficiently while modifying new procedures. Make all the employees aware of ISO in Ghana regarding efficiency and quality standards.
Initial Certification Audit
It is divided into two groups:
Stage 1
Stage 2
Stage 1:
ISO Consultants will audit any changes you make to the organization in Kumasi. Your systems and procedures will be evaluated for possible non-conformities to the quality management system. Non-conformities will be divided into major and minor ones. By modifying the association’s processes and techniques, the applicant must order all these non-conformities according to the desired quality standards.
Stage 2
After all the important changes are done in the Organization, the ISO audit in Ghana does the final auditing. ISO auditor in Ghana will check whether all the non-conformities have been canceled or not as per ISO quality standards. If the ISO auditor is self-satisfied, they will prepare and forward the final ISO audit report to the registrar.
Completing the ISO Certification in Ghana
After all, non-conformities are forwarded to the registrar, and all findings are included in the ISO audit report; the registrar will assist you with the ISO Services in Ghana.
The cost involved in the ISO Certification Process in Ghana.
ISO Services in Ghana are not fixed-priced, and costs vary from Organization to Organization. After considering various boundaries, the ISO agency calculates ISO Cost in Ghana for each organization individually.
The number of processes
Employees
The risk level associated with the association’s scope of services
The complexity of the management system
The number of working shifts etc.
In Ghana, which industries are eligible for ISO certification?
Educational Companies, Trading Companies, Oil&gas Companies, Aerospace Companies, Trust/NGO Companies, Testing & calibration Companies, Fintech Companies, Construction Companies, Pharmaceuticals Companies, IT Design and Development Companies, IT services Companies, Services Industry Companies, Automobile Companies, Food Manufacturing Companies, Medical manufacturing Companies, Medical Laboratory Companies, Banking Companies, Logistics Companies, Accounting/ financial and consulting Companies, Manufacturing Companies, Trading Companies,
What is the best way to find ISO certification in Ghana?
Facrocert team is headed by able and experienced ISO Consultants in Ghana to provide ISO Consulting Services in Ghana. The company’s highly qualified and trained staff are committed to providing the best service to its clients. Ghanaian ISO Consultants offer a wide range of ISO Consulting Services, and their accreditation is recognized worldwide, as they are accredited for operations in major countries.
We provide the best ISO consultants in Ghana, Who are very knowledgeable and provide you with the best solution. And to know how to get ISO certification in Ghana? Kindly reach us at [email protected] ISO Certification consultants follow the guidelines set by the international organization for standardization and help the organization to implement ISO certification in Ghana in an easy way with proper documentation and audit.
For more information visit: ISO Certification in Ghana
Related Links: ISO Certification in Ghana
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Procedures to get ISO Certification in Iraq
Iraq ISO Certification Costs
Getting ISO certification in Iraq is not a fixed cost and varies from business to business. By considering various parameters, Genveritas ISO Consultants in Iraq can ensure an affordable cost for ISO certification:
An organization’s size
The number of employees
The number of processes
Risk level
Framework for administration
Work volume
Processing time for ISO certification in Iraq
Additionally, the time it takes for an ISO certification to be completed varies from business to business. Following a survey of the organization’s size, the ISO certification office can give reasonable consideration.
ISO Certification usually takes the following amount of time:
1-2 months for small businesses
3-6 months for medium-sized enterprises
Enterprises with a large workforce: 6-12 months
Procedure for Iraqi ISO Certification
1.The application/contract should be made.
The registrar and applicant should enter into a contract after selecting the ISO certification body and ISO standard. Liability issues, confidentiality, and access rights should be included in the application.
2. Document Quality Review
The ISO registrar will identify your quality manuals and reports with different approaches and strategies. Surveying existing work will enable the ISO registrar to identify potential gaps in the ISO standards against the prerequisites.
Arrangements should be made for action.
Your ISO auditor will convey the current holes in your organization, and you should set up an action plan to eliminate them. Develop a list of the tasks that must be performed to acquire the ideal organizational changes. Preparing your representatives to adjust to new methods while working efficiently may be necessary. As far as quality and productivity standards are concerned, ensure all representatives are aware of ISO standards ISO 22000 certification in Iraq.
Certification Audit
Initial ISO Certification Audits fall into two categories: Stage 1 and Stage 2
The onsite audit consists of the following:
The ISO auditor will inspect all your progress in the association. Attempt to recognize any possible inconsistencies between your frameworks and methods and the ideal quality management framework. There are two types of non-similarities: minor and major. Modify the association’s methods and procedures to adjust and carefully evaluate all these non-similarities under the ideal quality standards ISO 9001 certification in Iraq.
Audit results:
After all necessary organizational changes have been made, the ISO auditor performs the final examination. The auditor will check whether all non-congruities have been resolved according to ISO quality standards. After the ISO auditor has completed the final examination, they will prepare and submit the ISO audit report.
The ISO certification process has been completed.
The ISO registrar will grant you certification after all non-conformities are reviewed, and all findings are included in the Final ISO Audit report ISO 45001 certification in Iraq.
Audits relating to surveillance
The purpose of surveillance audits is to ensure that ISO quality standards are maintained within an organization from time to time.
For more information visit: ISO certification in Iraq
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ISO 14001 Certification Process in Dubai
ISO Certification process in Dubai Dubai's ISO 14001 Certification Process is less complicated, quicker, and more reasonably priced. The process for obtaining the certification will be greatly streamlined thanks to certvalue. Our goal is to help businesses quickly obtain ISO 14001 Certification in Dubai by offering affordable, competitive, and useful business solutions. Our strategy is straightforward and simple to comprehend. We are one of just a few specialised consulting firms with a global clientele and a service offering that includes all of the major international quality certifications, such as ISO, CE, HACCP, and CMMI.
Get in touch with us right away for a fair, free quote from our hardworking business development team. In accordance with your needs, we will create a detailed quote.
The OHSAS 18001:2007 Standard for Occupational Health and Safety (OHS) Management Systems is widely accepted.
The occupational safety and health hazard for the business can be managed comprehensively with the help of the 18001:2007 Standard. The OHSAS 18001 is made to help enterprises improve workplace safety, regardless of complexity or size.
The 18001:2007 Standard enables enterprises to show their dedication to a productive and safe workplace. The 18001:2007 Standard aids in detecting, assessing, and managing OHS hazards through the use of preventative measures.
The goal of OHSAS 18001 is to continually reduce workplace occupational hazard risk, which raises productivity for the business.
ISO 45001:2018 Certification in Dubai
Currently, ISO 45001: 2018 Certification is taking the place of OHSAS 18001:2007 Certification. ISO 14001 Certification services in Dubai The most recent Standard lays out practical guidelines for improving worker safety. The goal of the ISO 45001:2018 Standard is to lower the number of fatal accidents, minor workplace injuries, and lost workdays.
According to International Labour Organization (ILO) statistics from 2017, 2.78 million workplace fatalities occur each year. Additionally, 374 million minor injuries at work occur each year.
The structure of ISO 45001:2018 allows it to work with other ISO Quality Management Standards. Compatible with ISO 9001 (Quality Management) and ISO 14001, the new Standard (Environmental Management).
Organisations that have already achieved OHSAS 18001: 2007 certification are currently converting to the ISO 45001:2018 Standard. The migration standards for switching certification from OHSAS 18001:2007 to ISO 45001:2018 have been created and published by the IAF (International Accreditation Forum).
The OHSAS 18001:2007 Standard Certification and ISO 45001:2018 Standard Certification differ.
OHSAS 18001 will be replaced by the ISO 45001 Standard. Even though the ISO 45001 Standard draws heavily from OHSAS 18001, it stands alone and is not merely an update.
ISO 14001 Lead Auditor Training Dubai
ISO 14001 Audit in Dubai In order to create, implement, and maintain environmental management systems in enterprises, the ISO 14001 lead auditor training Dubai strives to emphasise the most recent standards and practises (EMS). In the Dubai ISO 14001 ems training course, candidates will understand how to evaluate ecological factors, impact, and solutions for putting continuous improvement techniques into practise. The methods and methodologies for auditing, such as audit planning and execution, audit summary creation, audit summary verification, audit summary nonconformity statement creation, and audit summary case study development, will be understood by the participants. Additionally, it serves as an example of how to develop a sustainable model by enhancing auditor abilities according to ISO 19011: "Guidelines for auditing management systems" and ISO 14001:2015. This course has been registered for and authorised by the IRCA's regulatory body.
ISO Consultancy in Dubai Certvalue, the top supplier of ISO 14001 Certification in Dubai, provides implementation services for ISO 14001 Certification in Dubai, Abu Dhabi, Ajman, Al Ain, and other key cities in Dubai. If you want to learn more about ISO 14001 certification in Dubai, get in contact with us. You will earn the certification by using our certvalue consultancy's assistance. Our consultants will be available for you whether you're staying in Abu Dhabi or Dubai.
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Why should the Manufacturing Industry Make Quality Audit a Routine?
Do you know that gaining insight from an internal audit report is a powerful catalyst for driving new revenue? Yes! A quality audit can help you reach your destination by improving the quality of the products you are manufacturing. Still, not ready to believe it? Ok, let me explain to you why most of the companies, dealing with manufacturing, are including quality audit in their routine curriculum.
Three most essential components of a Quality Management System (QMS) are- compliance, process, and product audits. These three components are required for a successful management strategy. Hence, these three components need to be audited frequently. A manufacturing company should garner data on these components. After gaining the data and giving them the form of an audit report, the market expert will be able to analyze the report and modify the manufacturing process or delivery procedure as per the customer response.
By performing a Quality Management Audit on a regular basis, an organization will be able to:
• Increase sales by making a correction to the flaws and improving the quality • Turn the sales bump into long-term sales acceleration • Adhere to the ISO 9001 Standard for availing greater employment and long-term sales growth
A research paper, “Quality Management and Job Quality: How the ISO 9001 Standard for Quality Management Systems Affects Employees and Employers” published by Harvard Business School, has revealed that periodic audits are critical for securing continual improvement.
Well, this is not the end! I am going to share with you five reasons ISO 9001 Quality Audit must be included in the routine of a manufacturing business. Let’s check them out:
1. An internal audit for Quality Management clearly defines and identifies the major and minor non-conformance by products and comes up with the actions required for resolving the issues
Often product quality issues give birth to a number of problems in the customer-business relationship. With the help of periodic audit, a business can track the major or minor conformances existing in the product quality.
The internal auditors first capture the trending data based on the noncompliance or the corrective actions to score the nonconformities with an ideal Quality Management System. This way, the company will be able to identify and address the quality issues immediately.
A manufacturing business needs a fresh set of data on these areas every month or at least once in three months. It implies that you need to conduct an ISO 9001 internal audit every month or at least once in three months.
2. Internal audit plays an indispensable role in developing a manufacturing intelligence knowledge-based tracking method for quality performance
The manufacturing industry has been constantly insisting on Manufacturing Intelligence. It is designed with data capture, aggregation, and advanced analytics. A better audit report will be rich with detailed and robust information.
Having reliable data in place, the manufacturing Intelligence applications will be able to provide you with insights into the points of the product. It enables you to process weaknesses, which might not be visible before the internal audit. It will enable the organization to gain new insight into the possible quality challenges, which would affect the quality performance in the future. Moreover, a quality audit helps an organization take proper initiatives in an advanced stage to avoid any pitfalls.
3. Quality audit maintains the highest level of health and safety plant-wide while keeping injuries down by employing the best audit methods for tracking and improving the current state
An internationally acclaimed high-tech manufacturer will always conduct a quality management audit every 60 days to measure health and safety compliance. This frequent internal audit will help them reach the highest level of safety and slow down the sudden accident within the organization. As an outcome, the organization will be able to motivate their existing employees and encourage potential candidates to join the organization.
4. An internal audit for ISO 9001 Standard provides improvement recommendations based on recent audit data Since an internal audit inspects the entire quality management system and points out the loopholes, it can act as the best guidelines for improving the quality. Based on the data stated in the internal audit report, the internal auditors will make recommendations for further improvement.
5. ISO 9001 Quality Audit keeps the Key Performance Indicators or KPIs at the center of the audits and track how operations plant-wide work against the plan
Sometimes, the most valuable audits can effectively detect where the internal disconnects are affecting the customer lost time, orders, and potential to produce more revenue on their own.
Endnote
When you are into the manufacturing business, you must embark on a journey to the highest quality. This is the best way of retaining existing customers and drawing the attention of new potential customers. Internal audit is the best way of analyzing the current state of the business and find out the loopholes for ensuring further improvement and consistency.
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#iso 9001 bas denetim sorulari#iso 9001 uygunsuzluk listesi#iso 9001 audit checklist#iso 9001 major minor#kalite yonetim kontrol listesi#iso 9001 denetim sorulari 2024#iso 9001 quality audit#iso 9001 denetim raporu#iso 9001 sertifikasyon#iso 9001 ic denetim#iso 9001 uygunsuzluk tespiti#kalite yonetim sistemi egitimi#iso 9001 uygunsuzluk raporu#iso 9001 sertifika denetimi#kalite denetim sorulari#iso 9001 denetim standartlari#iso 9001 belgesi nasil alinir#iso 9001 denetci kontrol listesi#iso 9001 denetim kriterleri#iso 9001 ic denetim proseduru#iso 9001 belgelendirme denetimi#iso 9001 performans denetimi#iso 9001 surec denetimi#iso 9001 denetim adimlari#iso 9001 surec yonetimi
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Process of ISO Certification
ISO Certification in Saudi Arabia alludes to Worldwide Association for Normalization. An autonomous association gives norms with regard to the quality, security, and proficiency of items and administrations given by organizations. With the rising contest among the business, it is essential to convey a great of products and administrations to support on the lookout. ISO affirmation assists with further developing your business believability as well as by and large proficiency of the business.
Pre-Imperative to ISO Affirmation Cycle in India
Picking the sort of ISO Confirmation
Above all else, you want to pick the sort of ISO confirmation expected for your business. There are different sorts of ISO certificates accessible, for example,
ISO 9001 2008 - Quality Administration
ISO 14001 - Ecological Administration
ISO 27001 - Data security The board
ISO 22008 - Food handling The board, etc.
Picking an ISO Affirmation Body
It should be noted that ISO itself doesn't give affirmation to the organizations. Affirmation is finished by the outside bodies. You really should pick a perceived and believable accreditation body. While picking the ISO enlistment center, you ought to remember the accompanying:
Assess a few ISO Confirmation specialist organizations.
Check to assume they are adhering to the CASCO guidelines. CASCO is the ISO board that takes care of problems connecting with similarity evaluation.
Check regardless of whether it is certified. Certification isn't necessary however they should meet the prerequisites of ISO Authorization bodies.
Process for ISO Accreditation in India
Make an application/contract
The candidate and the recorder ought to settle on an agreement. This agreement generally characterizes the privileges and commitments of the two players and incorporates risk issues, secrecy, and access freedoms.
Quality Reports Survey
The ISO examiner will see all your quality manuals and records connected with different approaches and strategies being continued in the association. A Survey of existing work will help the ISO reviewer to distinguish the potential holes against the prerequisites specified in the ISO principles.
Make an Activity Arrangement
After the ISO evaluator imparts the current holes in your association, you ought to set up an activity intend to dispose of these holes. Set up the rundown of the expected undertakings to be performed to get the ideal changes for your association. You might be expected to give preparing to your representatives to work effectively while adjusting to new methods. Make every one of the representatives mindful of the ISO principles concerning work effectiveness and quality norms.
Starting Confirmation Review
The underlying confirmation review is separated into two classifications Stage 1 and Stage 2.
Stage 1: The ISO evaluator will review the progressions made by you in the association. They will then attempt to recognize the conceivable non-similarities in your frameworks and strategies to the ideal quality administration framework. They will isolate these non-similarities into minor and major non-congruities. The candidate should cautiously evaluate every one of these non-similarities and get it adjusted according to the ideal quality guidelines through a change in the strategies and cycles utilized by the association.
Stage 2: After every one of the necessary changes is finished in the association, the ISO examiner does the last review. The inspector will check regardless of whether all the non-congruities have been killed according to ISO quality guidelines. On the off chance that the ISO reviewer is fulfilled, they will set up the last ISO review report and forward it to the enlistment center.
Finishing the ISO Affirmation
After all, non-similarities are tended to and every one of the discoveries is placed in the ISO review report, the recorder will concede you the ISO affirmation.
Observation Reviews
Observation review is fundamentally directed to guarantee that ISO quality principles are being kept up with by the organization. It is led now and again.
Cost engaged with the ISO Confirmation Interaction
The cost of getting ISO Services in Bahrain affirmation isn't fixed and shifts from one association to another. The ISO affirmation office works out the expense of ISO confirmation independently for every association in the wake of thinking of them as on various boundaries.
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Nilesh Vedak managing director Syntegon India
In light of Bosch divesting its packaging business globally several years ago, and the business now branded as Syntegon, Packaging South Asia editor Naresh Khanna tried to understand if and what changes may have come to the company’s substantial Indian operations which include manufacturing in a purpose built modern factory in Verna in Goa. Syntegon India’s managing director Nilesh Vedak gives us some straight answers.
Packaging South Asia – What if any are the major changes in Syntegon in India in light of the company being divested by Bosch?
Nilesh Vedak – There have been no major changes. Verna continues to be an important Syntegon site, and the company keeps investing in its facilities to meet the increasing demand of domestic and international markets. With 150 well-qualified and experienced employees and an installed base of over 3,000 machines in India and overseas, Syntegon is one of the top players among the packaging machinery manufacturers.
PSA – What are the machines being manufactured in India at the Goa plant?
Nilesh Vedak – Syntegon’s facilities in India are certified according to the ISO 9001: 2015 norm and manufacture primary and secondary packaging machines for the food and non-food industry, including vertical baggers, horizontal wrappers, and various feeding solutions as well as a range of cartoners for automated packaging processes and process technology for confectionery products.
PSA – What are the major or minor or interesting sales that are taking place in the Indian and nearby markets for the Syntegon Indian team?
Nilesh Vedak – We do not disclose our current sales projects to ensure the privacy of our customers. However, Syntegon is involved in numerous customer projects in India, which we will reveal as soon as they are market ready.
PSA – We may be wrong but we sense or see a change in alignment of Syntegon in Europe with pharma packaging machines, is that also reflected in India or are you still selling and supporting pharma packaging machines in India?
Nilesh Vedak – Syntegon is still manufacturing and selling packaging equipment in India. As far as pharma machines are concerned, the focus is on the entire production and primary packaging process for liquid and solid pharmaceuticals, as well as on services along the entire machinery lifecycle. The food portfolio focuses on vertical baggers, horizontal wrappers, and various feeding solutions as well as a range of cartoners for automated packaging processes and process technology for confectionery products.
PSA – What if any role has Syntegon played in the Covid-19 vaccine delivery program in India and for exports?
Nilesh Vedak – Syntegon offers complete line solutions and is an important partner of pharmaceutical manufacturers worldwide. Our customers rely on our packaging, processing, filling, and inspection technology to produce safe vaccines. We support them with fast-track line configuration and a comprehensive service portfolio to retrofit or modernize their existing machines. Qualification and documentation further support pharmaceutical manufacturers in delivering safe vaccines.
PSA – Any new Indian-made machines for food and beverages?
Nilesh Vedak – Among other solutions, we recently showcased three new machines at Syntegon’s in- house customer show in India. These are –
- A high-speed vertical bagger specifically designed for the snacks market which is highly cost- sensitive and fragmented (Terra 25 HS). The bagger delivers optimal efficiency and supports manufacturers in remaining competitive. The compact, versatile and operator-friendly machine is equipped with belt draw-off technology with a servo cross sealing system to ensure accurate single and chain bags with quality seals for a robust design.
[caption id="attachment_68956" align="alignright" width="300"]
Sigpack TTM has a quick vertical restart and optimal flexibility[/caption]
- A vertical bagger (SVZ 1803) designed for packaging abrasive and corrosive products such as salt. Corrosive substances need to be handled very carefully during processing and packaging. Salt particles for example tend to stick to the forming tube and the packaging material causing slippage of film in belt driven machines. That is why the machine is equipped with jaw draw-off technology with servo cross sealing system to ensure accurate bags with quality seals for a robust design.
- A cartoner designed for 24/7 production and optimal OEE (Sigpack TTME). Thanks to its patented tool-less changeover concept, the machine has a quick vertical restart. The cartoner also offers optimal flexibility as it is designed to handle diverse packaging styles and formats and materials and can be scaled up to 30 cartons or 800 products per minute to fit manufacturers specific production capacities
PSA – What are the packaging filling and sealing trends in India, particularly for food, confectionary, baking, beverages and for pharma?
Nilesh Vedak – Sustainability continues to be a major trend in the food industry worldwide, as a growing number of consumers demand eco-friendly alternatives to their everyday products. It is therefore becoming increasingly important for food manufacturers to be able to process conventional as well as alternative packaging materials such as paper or fully recyclable mono-materials. In addition, the pandemic has fueled the trend towards automation, especially when secondary packaging is concerned.
By increasing the level of automation in their packaging lines, food manufacturers are able to achieve more flexibility and efficiency as well as meet highest hygiene standards. In India specifically we see a rise in demand for sophisticated bag styles such as the doy style or full corner seal styles. In pharma applications, the focus is on speed and flexibility in the choice of pack styles and fast product changeovers. Fast time-to-market is especially important for new drug developments. Syntegon offers equipment and services for all these needs.
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False Ceiling Services: Things to Keep in mind While getting False Ceiling Done
Number 1: Be Clear About the Loads to be Endured Number 2: Be Clear About your Priority Number 3: Ask for Sample Panels
False Ceilings are ubiquitous, both in industries and in residential houses. With plenty of materials and service providers at your disposal to choose from, it becomes too easy to lose focus and commit minor, but expensive, mistakes. So, here are three checklists to tick off while employing false ceiling services.
Panels are built to withstand a certain amount of load, exceeding which may result in panel failure. Metal panels may bend and bulge, while PUF or PVC panels may downright rupture when faced with exceeding loads. To avoid any future damage to components, be clear about the provisions going to be mounted or supported by the false ceiling with your contractor. Not exact figures are needed but the provider must have a clear idea about the approximate weight needed to be supported.
False ceiling services vary as per their purpose. While many panels can be employed to fill several demands, it is usually best to choose one panel that excels at fulfilling your major requirement. Case in point, if you prioritize fire safety just go for VATSON Fire Resistant Panels (Class 4880 FM Global Approved) or similar fire-resistant panel. If you want thermal insulating materials, just go for VATSON Duoroof ® Panels or similar panels. It's always advisable to pick a specific panel instead of a generic one.
While one can read specs, and view pictures, it's best to check the panels with your hands. Simple tests such as visual inspection, knocking, bending, hammering can be used to determine the build quality and strength of the panels
How can VATSON Help You?
VATSON, an ISO 9001: 2015 certified company, has 26+ years of experience providing false ceilings services to more than +150 satisfied clients. We offer services suited to your requirements, such as Vatson Fire-Resistant Panels, capable of enduring extreme temperatures for as long as 2 hours, or Vatson Rockwool ® Green Panels, which are up to 99% biodegradable. No matter what the project is, we are there to help.
For a consultation about the Walkon ® Walkable False Ceiling and related services, Email at: [email protected] or reach out by calling +91-40-2779-5506.
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Why is Non-Conformance Management important?
Article Context:
Non-Conformance Management
Non-Conformance Types
Why Non-Conformance Management is Important ?
Consequences of an Non-Conformance Failure
Introduction
FDA and ISO have a defined set of guidelines to enable organizations to handle their quality processes effectively.
Non-Conformance according to ISO 9001:2015The organizations certified for ISO 9001 are expected to ensure error-free quality processes and stringent mitigation plans to handle errors. In addition, the regulations mandate regular quality checks through internal and external audits to comply with efficient and better product delivery.
Non-conformance management is one of the crucial elements in the quality process management lifecycle.
Non-Conformance Types
Non-Conformance is categorized into two types – Minor Non-Conformance and Major Non-Conformance.
Minor Non-Conformances are slight deviations that occur in a product, process, or service. It is less obstructive as it does not cause a problematic scenario for the organization. But it is essential to investigate and resolve an Non-Conformance, no matter how negligible the impact is. More often than not, the minor issues have been ignored that led to critical problems and failures. A minor Non-Conformance, when ignored, could lead to CAPA. So, there is a need for the organization to address immediately to avoid systematic issues in the future.
Major Non-Conformance, on the other hand, is often critical and might lead to a CAPA. In addition, major Non-Conformance has higher chances to impact the credibility and reliability of the organizations.
Reasons Why Non-Conformance Management is Important
The Non-Conformance management process aims to identify, investigate, and resolve Non-Conformance’s and document the Non-Conformances report. Also, examine the patterns of issue occurrences and help management streamline Corrective and Preventive Action to prevent recurrences and stay compliant with the regulations.
It helps the organizations identify the defects in products or processes and identify the critical issues that were to occur in the future.
It acts as a performance indicator of deficiencies, systematic issues, and operational procedures in place.
With critical documentation of Non-Conformance logs, organizations have the opportunity to identify patterns and promote better corrective and preventive measures and enhance proactive risk assessment.
Aids in delivering quality products and services improving customer satisfaction and company revenue.
A functional Non-Conformance Quality Management Software allows the users to stay connected with the quality process. Non-Conformance is not just a quality procedure of an organization; it is the core responsibility of users to report and handle potential NC to prove their quality of work.
Consequences of an Non-Conformance failure
The above explains why non-conformance management is essential. Now, let us know what the consequences of a Non-Conformance are is ignored or failed to manage. The first and crucial is that Non-Conformance process negligence leads to product failures and increases product recalls frequency and customer dissatisfaction. It incurs production and operational costs. A continual trend of development recalls, complaints, poor procedures can harm patient health and consumer health. The whole point of handling non-conformances is not only the reputation of an organization; it is for the safety of humans using those devices and medicines. Deficient performance of an organization in audits leads to falling reputation and would further lead to cancellation of ISO certification or hinder from being ISO certified.
The below is the pictorial representation of a functioning NC Management Process
Identification >>>> Initiate (document the information, identify for major or minor Non-Conformance, define why it occurred) >>> Investigation (Deep dive into the problem and identity what led to the non-conformance occurrence) >>> Actions (Review the findings, check the process gaps, decide the actions that are required to resolve the Non-Conformance and to prevent the same issue from occurring in future. A few of the common dispositions that arise during a Non-conformance management – Raise a CAPA, No CAPA but other actions required, no actions) >> Review (Once all the information has been documented, send over the analysis to the manager for approval) >>> Implementation < Once approved, implement the Non-Conformance actions) >> Verification (verify the executed actions) >>> Close Non-Conformance once the verification is a success.
Digitizing Non-Conformance
Handling non-conformances via paper-based processes might seem easy initially. However, an increase in the volume of data would lead to a lot of pain points. A few ways in which digitizing your non-conformance can help are:
Retrieving years old non-conformance for audit might take a longer time. There is a higher risk of misplacing physical documentation
Missed insights – What if most of your non-conformances in the previous years were because of a single supplier, and you could not connect the dots due to disparate paper-based data?
Adherence to policy – Digital processes help you apply constraints that make it impossible to progress unless the required data is filled and help in reducing human errors/misses.
iQuality’s design to ensure seamless Non-Conformance management process
iQuality’s Quality Management Software holds a set of features that enable the employees of the life science industry to handle their non-conformance processes effectively. The Quality Management tool with close-loop configurable workflow helps companies organize their Non-Conformance process and documentation better. Furthermore, the quality tool provides traceability and visibility of information documented with just a click across the organization. It also provides actionable insights through analytics-powered reports.
Would you like to know more about managing and streamlining the Non-conformance process in your organization? Contact [email protected] to discuss your needs?
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The most effective method to profit from three unique sorts of Quality Management Inspections
We've set up that low quality can be unfavorable to your main concern and production network permeability is vital to overseeing quality control. Performing investigations during the production cycle prevents low-quality items from leaving the industrial facility. Auditors should catch and resolve quality issues before they harm a brand or retailer's primary concern or reputation.
The Three Types of Quality Inspections
There are three essential sorts of value investigations: pre-production, in-line, and final. There is an assortment of subtleties that should be examined and supported during each stage to recognize and address quality issues.
Pre-production Inspection
During ISO 9001 Certification the pre-production stage, unrefined components need to be tried before entering production. This might incorporate various tests to inspect the material for weight, layered strength, pilling opposition, stock maintenance, stretch recovery, and considerably more. Parts including terminations, zippers, elastics, and different embellishments, for example, beads, sequins, and bolts need to likewise be tried for administrative prerequisites.
Since quality issues are frequently an aftereffect of deformities in the materials, assessments during the pre-production stage permit auditors to resolve any issues before production starts. At last, by assessing the materials front and center, brands and retailers can stay away from unforeseen expenses and postponements.
Also, Check --> ISO 9001 Certification Principles
In-line Inspection
Extra examinations should happen during different phases of production as per ISO 9001 Certification guidelines. For apparel, reviews need to happen at each basic advance of the production cycle, from slicing to collecting to squeezing or other completing methodology. For instance, during the cutting stage, each cutting ticket need to be randomly examined to guarantee that each part is precisely indented and conceals are isolated. Assuming texture is inaccurately cut, the parts can't be as expected collected.
In-line investigations are significant, as quality issues are frequently re-useful during the production stage and can be fixed before the eventual outcome is finished. At the point when quality issues are not rectified during the production cycle, minor issues at the start of production can prompt bigger issues in later stages.
Final Inspection
The last examination is the last chance for evaluators to catch and resolve quality issues before they end up in the possession of the purchaser, or far more even worse, the buyer. During the last review, items are inspected for explicit execution necessities, generally speaking, appearance, measuring, and fit.
Brands and retailers frequently skip examinations while the items are currently at the manufacturing plant and just perform arbitrary, final inspections once the order is received at the ultimate destination. By then, at that point, it is past the point of no return and the main plan of action is disposing of the low-quality units. This is exorbitant to each party, particularly the processing plant, which will endure the worst part of the cost.
Also, Check --> ISO 9001 Standard Certification: What Is It and How it helps you?
Work on Inspections with Quality Control
Quality Control arrangement answers for examiners to play out each of the three sorts of examinations before the request ships. ISO 9001 Certification compliance highlights the disconnected abilities with worldwide coordinated effort in different dialects. The framework permits reviewers to lead different investigation types per PO, take photographs of deformities, and produce the Corrective Action Plan. It upholds different imperfection levels (minor, major, basic), and single and two-fold inspecting plans. All the data gathered on the tablet is transferred to the brand or retailer's store network the management arrangement, bringing about constant revealing and disappointment warnings.
To more deeply study how Quality Management can assist with improving on your review processes, or to demand a demo, if it's not too much trouble, reach us.
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Best Accuracy in Toughest of Terrains
SATPALDA has created a Digital Terrain Model (DTM) of an area which is covered with steep hills, multiple streams and a major river on its eastern side. The presence of dense vegetation at several places was a challenge to determine the best elevation. The terrain had an elevation range between 1428 m to 5521 m. This was neither a software generated process nor an algorithm based solution.
Our skilled and experienced team of photogrammetry engineers digitized the terrain with breaklines and all other features like rivers, roads, streams and ponds. It was a well-planned project with a defined methodology and checklist for the production and quality process. Eight GCPs were used to control the area which was later used to validate the DTM.
Results Achieved
With the creation of this product, SATPALDA has shown its capability to work on the toughest of terrains which are covered with dense vegetation. Due to our in-depth expertise and experience to handle every minor and major terrain change, the highest quality DTM was delivered to the customer within the stipulated time frame which has a far better accuracy than what was committed.
Accuracy Achieved
Vertical accuracy at 95% confidence level : 30cm Horizontal accuracy at 95% confidence level : 25cm
“SATPALDA is an ISO 9001:2008 certified leading provider of geospatial products and services. The company is also a reseller of multiple satellite data products and has a proven track record of delivering project-critical geospatial products, including satellite imagery, UAV imagery, elevation models, LULC maps, planimetry, terrain solutions as well as innovative solutions such as countrywide datasets and Airport Mapping solutions. With an experienced team having thousands of man hours of project experience and expertise, the company focuses on providing value-based solutions to its customers in a time bound manner. As a responsible social entity SATPALDA strives to promote the latest Geospatial technologies to support critical issues such as climate change, environment and security etc.”
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USQC offers a proven path to certification, backed by numerous years of industry experience. Whether your quality management system is in need of major or minor changes, our approach helps to foster quality commitment within your organization from the top down. Certification to quality specifications (e.g., ISO TS29001, ISO 9001, ISO 14001, ISO 45001, ISO 13485, ISO 29001). visit www.USQC.us or contact : [email protected] #usqc #safety #quality #maritime #petroleum #oilandgas #courses #certification #HACCP #6sigma #sixsigma #followforfollowback #follow #follow4like #iso #iso9001 #transition #iso44001 #iso17100 #ascaccredited #americanquality #gmp #CERTIFICATION #isocertificate #isocertificationbody #isocertification #iso22000 (at New Jersey) https://www.instagram.com/p/CQ5DvlVrCbR/?utm_medium=tumblr
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ISO CERTIFICATION IN NIGERIA
Nigeria is a country in West Africa. It adjoins Niger in the north, Cameroon in the east, and Benin in the west. Its southern seaboard is on the Gulf of Guinea in the Atlantic Ocean. Nigeria is a federal republic containing 36 states and the Federal Capital Territory, where the capital city Abuja, is located. Lagos is one of the largest cosmopolitan areas in the world, is the most populous city in Nigeria and the region of Africa.
Nigeria has the largest economy in Africa; its re-emergent manufacturing sector became the largest on the continent in 2013, and it provides a large portion of goods and services for the West African subcontinent. Nigeria contributes only about 2.7%(percent) of the world's oil supply. Although the oil division is essential, as administration funds still heavily rely on this division, it endures an inadequate part of the country's overall economy.
The large maintenance of the agricultural sector has not kept up with speedy population growth, and Nigeria, once a large net exporter of food, now imports some of its food commodities, though trade has led to a resurgence in production and exporting of food commodities, and the movement towards food supply.
Procedure for ISO Certification in Nigeria
1. Make an application record
Once the industry owner has decided to choose the ISO 9001 certification in Nigeria and other ISO standard bodies, the registrar and the applicant should agree on a contract deal. The statement should include the advantages and responsibilities of both individuals and holds compulsion effects, confidentiality, and access benefits.
2. Quality Documents Review
The ISO registrar will see all your quality guidebooks and statements recognized with various procedures and policies being followed in the company. The Survey of subsisting work will assist the ISO registrar to identify the possible gaps against the requirements specified in the ISO standards.
3. Make an Action Arrangement
After the ISO auditor carries the current gaps in your organization, you ought to set up an exercise expected to carry out those gaps. Set up the outline of the essential tasks to be implemented to obtain the absolute changes in your federation. You might be expected to provide your deputies to operate proficiently while conforming to fresh techniques. Make every one of the deputies attentive to the ISO standards as considerably as work potency and quality measures.
4. Certification Audit
Primary ISO Certification Audit is partitioned into two classifications Stage 1 and Stage 2.
Onsite Audit:
The ISO auditor will monitor all the improvements performed by you in the organization. At this point endeavor to identify the credible non-congruities in your structures and approaches to the perfect quality management structure. The command partition certain non-similarities into minor and major non-congruities. Notice all these non-similarities balanced and accurately estimated according to the absolute quality measures through modification in the processes and systems utilized by the organization.
Final Audit:
ISO auditor does the final analysis after all the required adjustments are done in the organization. The auditor will review whether all the non-congruities have held inclined or not according to ISO quality measures. Once the ISO auditor is accomplished by the final review, they will set up the ISO audit report and deliver it to the ISO registrar.
5. Finishing the ISO Certification
After all, the non-conformities are examined and every one of the discoveries is offered in the Final ISO Audit report, the ISO registrar will impart you the ISO certification in Nigeria.
6. Surveillance Audits
Surveillance Audit is managed from period to period basically to confirm that ISO quality measures are being sustained by the industry.
Cost of ISO Certification in Nigeria
The cost of obtaining ISO certification is not fixed and alternates from industry to industry. We Finecert Solutions ISO Consultants in Nigeria can obtain certain of the affordable cost for ISO in Nigeria by analyzing multiple parameters:
1. The size of an organization
2. Number of workers
3. Number of Processes
4. Level of hazard
5. The Administration framework
6. The quantity of work
Services from Finecert
Having described various types of ISO Standards and the advantages of obtaining ISO certified, one query that arrives in mind is that how does one gets these certifications for their organizations.
Finecert Solutions strives in giving businesses all-around support from consultation to implementing certifications that are internationally trusted, cost-effective with hassle-free methods.
Finecert is a team of skilled professionals who expertise in serving the complete procedure at a very economical price which adds extreme worth to any business. ISO Cost in Nigeria at a very minimal price as we put in great effort to perform this by focusing on each concern and forming a solid partnership with our clients. Understanding and implementing the various ISO standards certification to any business/company has always been quite a challenging procedure. But, Finecert does it with ease.
Discover some of the globally accepted best-known and most widely-used standards, visit www.finecert.com For any queries, write to us at [email protected].
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