#ILAC-MRA

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How to Choose the Right Laboratory for Medical Tests in Jaipur

When it comes to medical tests, choosing the right laboratory is crucial for accurate results and a positive healthcare experience. With numerous diagnostic centres providing all types of medical tests, including CBC tests, liver function tests, and thyroid profile tests, at an affordable thyroid profile test cost in jaipur, it is important to know how to select the best option.

Here are the things to consider when choosing the right laboratory for medical tests in Jaipur:

Accreditation

If a person wants to get accurate and reliable test results, choosing a laboratory that is accredited by recognised organisations such as the National Accreditation Board for Testing and Calibration Laboratories (NABL) and ILAC MRA is important. These laboratories adhere to quality standards and follow proper testing protocols. A wrong test result can cause serious difficulties, and cost individuals money, their health, and even their lives. Diagnostic test results errors can have devastating effects because they are used by doctors to recommend treatments or medications. You could save lives by selecting the most reputable lab.

Equipment and Technology

Medical science has seen great evolution over time. Nowadays, top laboratories in Jaipur have state-of-the-art technology that eliminates any chance of error in medical reports. Choose a medical lab that has advanced medical equipment that ensures precise testing.

Range of Services

Top laboratories in Jaipur offer a range of services, including radiology (X-ray, OPG, and BMD) and diagnostic services (ECG, TMT, and holter). In case a person needs to take additional medical tests or services, they should have the option to get these services in one place. Patients can save time and energy by selecting a lab that offers a variety of tests all under one roof. This enables them to get all the support they need without having to go here and there.

Expertise of Staff

The expertise and qualifications of the laboratory staff play a crucial role in getting accurate and reliable test results. Look for laboratories that employ highly skilled and experienced professionals, including pathologists, radiologists, microbiologists, and technicians. The lab technicians should have proper qualifications and knowledge in their respective fields.

Accuracy of the Report

Many laboratories in Jaipur offer test reports within 48–72 hours. They make sure that test reports are accurate and reliable. A person should always do their due research about the authenticity of the laboratory. This can be done by doing online research and reading patient reviews.

Final Words

Getting proper medical care is very important for any individual. This is why choosing the right laboratory is important. One can find top laboratories in Jaipur that offer hundreds of test reports and have multiple centres. Nowadays, one can also call for at-home test sample collection, which is offered by renowned laboratories. 

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NABL ISO 17025 Overview

(NABL) is an autonomous body under the aegis of Department of Science & Technology, Government of India, and is registered under the Societies Act. NABL has been established with the objective to provide Government, Industry Associations and Industry in general with a scheme for third-party assessment of the quality and technical competence of testing and calibration laboratories. Government of India has authorized NABL as the sole accreditation body for Testing and Calibration laboratories.

In order to achieve this objective, NABL provides laboratory accreditation services to laboratories that are performing tests / calibrations in accordance with ISO/IEC 17025 and ISO 15189 for medical laboratories.

These services are offered in a non-discriminatory manner and are accessible to all testing and calibration laboratories in India and abroad, regardless of their ownership, legal status, size and degree of independence.

NABL has established its Accreditation System in accordance with ISO/IEC 17011:2004, which is followed internationally. In addition NABL has to also comply with the requirements of APLAC MR001, which requires the applicant and the accredited laboratories to take part in recognized Proficiency Testing Programs in accordance with ISO/IEC Guide 43.

An applicant laboratory has to satisfactorily participate in at least one Proficiency Testing program, while the accredited laboratories are expected to cover the major scopes of accreditation in a cycle time of four years. Towards this objective,

EVOLUTION OF NABL

NABL had undergone the first peer evaluation by a 4 member team of APLAC in July 2000, based on which NABL qualified as an APLAC MRA (Mutual Recognition Arrangement) Partner as well as a Signatory to ILAC Arrangements. NABL was reassessed in July 2004 & July 2008 and as stated earlier the signatory status of NABL within APLAC MRA has been confirmed for further four years i.e. October 2012.

This distinction has brought additional responsibility on NABL and its accredited laboratories. Annual Surveillance is carried out to ensure that the accredited laboratories are continuing to comply the accreditation criteria. NABL and its accredited laboratories are also required to meet the new challenges arising out of requirements such as satisfactory participation in a recognized Proficiency Testing Programme and the requirement of estimating the Uncertainty in Measurements even by the testing laboratories. NABL has already published the revised guideline on Estimation of Uncertainty in Measurement for Calibration Laboratories.

Scope Of NABL ISO 17025

NABL ISO 17025—International Standard specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods.

TESTING LABORATORIES

Biological

Chemical

Electrical

Electronics

Fluid-Flow

Mechanical

Non-Destructive

Photometry

Radiological

Thermal

CALIBRATION LABORATORIES

Electro-Technical

Mechanical

Fluid Flow

Thermal & Optical

Radiological

MEDICAL LABORATORIES

Clinical Biochemistry

Clinical Pathology

Haematology and Immunohaematology

Microbiology and Serology

Histopathology

Cytopathology

Genetics

Nuclear Medicine (in-vitro tests only)

NABL ISO 17025 Certification Implementation Training

We are ISO 17025 consultants offering a customized training program on NABL 17025 for organizations.

ISO 17025 Implementation Benefits

Formal recognition of competence of a laboratory by an Accreditation body in accordance with international criteria has many advantages:

Potential increase in business due to enhanced customer confidence and satisfaction.

Savings in terms of time and money due to reduction or elimination of the need for re-testing of products.

Better control of laboratory operations and feedback to laboratories as to whether they have sound Quality Assurance System and are technically competent.

Increase of confidence in Testing / Calibration data and personnel performing work.

Customers can search and identify the laboratories accredited by NABL for their specific requirements from the Directory of Accredited Laboratories.

Users of accredited laboratories will enjoy greater access for their products, in both domestic and international markets, when tested by accredited laboratories.

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Kiểm nghiệm bao bì thực phẩm | Tư vấn – Kiểm nghiệm | Trọn gói – Chuyên nghiệp – Nhanh chóng

BAO BÌ THỰC PHẨM LÀ GÌ?

Bao bì thực phẩm là một sản phẩm công nghiệp, được dùng để chứa đựng, bao gói thực phẩm. Bao bì thực phẩm bảo vệ giá trị của thực phẩm, giữ cho thực phẩm sạch sẽ, an toàn, thuận tiện cho việc vận chuyển và quá trình bảo quản. Người tiêu dùng cũng dễ dàng sử dụng, tiêu thụ sản phẩm hơn.

Bao bì có thể coi là cầu nối giữa nhãn hàng và người tiêu dùng. Nó đại diện cho thương hiệu, thể hiện hình ảnh của công ty thông qua sản phẩm bên trong, cũng như thể hiện 1 cách trực quan nhất các thông tin của hàng hóa để người tiêu dùng có thể dễ dàng theo dõi và lựa chọn.

TẠI SAO PHẢI KIỂM NGHI���M BAO BÌ THỰC PHẨM?

Căn cứ pháp lý

Cơ quan chức năng đưa ra các quy chuẩn về chất lượng bao bì thực phẩm nhằm đảm bảo sức khỏe cho người dân. Theo quy định, chỉ tiêu tiêu chuẩn kiểm nghiệm bao bì thực phẩm được quy định như sau:

QCVN 12-1:2011/BYT : Quy chuẩn kỹ thuật quốc gia về an toàn vệ sinh đối với bao bì, dụng cụ tiếp xúc trực tiếp với thực phẩm bằng nhựa tổng hợp.

QCVN 12-3:2011/BYT : Quy chuẩn kỹ thuật quốc gia về an toàn vệ sinh đối với bao bì, dụng cụ tiếp xúc trực tiếp với thực phẩm bằng kim loại.

QCVN 12-2:2011/BYT :  Quy chuẩn kỹ thuật quốc gia về an toàn vệ sinh đối với bao bì, dụng cụ tiếp xúc trực tiếp với thực phẩm bằng cao su.

QCVN 12-4:2015/BYT: Quy chuẩn kỹ thuật quốc gia về an toàn vệ sinh đối với bao bì, dụng cụ tiếp xúc trực tiếp với thực phẩm bằng thủy tinh và gốm sứ.

♦ Xem thêm: Công bố sản phẩm thực phẩm nhanh chóng, đúng quy định pháp luật

Sức khỏe người tiêu dùng

Bao bì thực phẩm là sản phẩm tiếp xúc trực tiếp với thực phẩm. Nếu quá trình sản xuất không đồng nhất, có yếu tố mất an toàn vệ sinh, sản sinh các chất độc hại có thể khiến bao bì mang mầm bệnh lây nhiễm vào thực phẩm. Ngoài ra, quá trình sử dụng, bao gói thực phẩm trong bao bì có thể gây ra phản ứng độc hại không mong muốn, thôi nhiễm vào thực phẩm hoặc quá trình bảo quản chưa đúng cách gây ảnh hưởng xấu đến sức khỏe người tiêu dùng.

Trong thời đại xã hội phát triển, người tiêu dùng đã thận trọng hơn rất nhiều, không chỉ với thực phẩm mà với cả bao bì bao gói phía ngoài, cũng như các thông tin được in trên đó.

CHỈ TIÊU KIỂM NGHIỆM BAO BÌ THỰC PHẨM

Các chỉ tiêu kiểm nghiệm bao bì thực phẩm đã được quy định theo các quy chuẩn kỹ thuật tương ứng. Để xác định được chỉ tiêu, khách hàng cần phải nắm được sản phẩm của mình cần phải kiểm nghiệm theo quy chuẩn nào.

>> Với 4 quy chuẩn hiện hành liên quan đến bao bì thực phẩm, khách hàng có thể dễ nhầm lẫn và kiểm nhầm chỉ tiêu.

Hãy liên hệ với Hotline: 0965 338 523 để được VnTest hỗ trợ tư vấn.

ƯU THẾ KHI KIỂM NGHIỆM TẠI VNTEST

VNTEST đạt chuẩn mực công nhận quốc tế theo ISO/IEC 17025:2017 được công nhận bởi Văn phòng Công nhận chất lượng (BoA)– Bộ Khoa học và Công nghệ và thừa nhận ILAC-MRA bởi Hiệp hội công nhận phòng thí nghiệm quốc tế (ILAC) với mã công nhận là VILAS 1296.

Với đội ngũ kiểm nghiệm viên có tay nghề cao và nhiều kinh nghiệm, cùng hệ thống trang thiết bị thử nghiệm hiện đại, phong cách làm việc chuyên nghiệp, chúng tôi luôn sát cánh cùng người tiêu dùng và nhà sản xuất để giảm thiểu nguy cơ rủi ro, bảo vệ lợi ích khách hàng. Nguồn: https://vntest.vn/dich-vu-kiem-nghiem-bao-bi-thuc-pham/

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R304 – General Requirements: ISO 17034 Reference Material Producer Accreditation Program R307 - General Requirements - Accreditation of ISO-IEC 17065 Product Certification Bodies R311 - Specific Requirements - Federal Risk and Authorization Management Program. ISO/IEC 17025 for Testing/Calibration Laboratories ISO 15189 and CLIA for Clinical Testing Laboratories. ISO/IEC 17020 for Inspection Bodies ISO/IEC 17043 for Proficiency Testing Providers. A2LA is governed by a Board of Directors. International Laboratory Accreditation Cooperation (ILAC) Mutual Recognition Arrangement (MRA.

The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required to our current documents?” or “What new documents do we need to generate to ensure compliance?” The ISO 17025:2017 standard actually requires fewer documents than the 2005 revision. In this article, you’ll find a snapshot of what documents you need to have to be compliant with the 2017 revision of ISO 17025.

Before joining Temasek, John was a Partner of TPG Capital (“TPG”), where he led the firm’s Technology Buyout Team for 17 years. Prior to TPG, he was a Managing Director and Co-Head, Technology Investment Banking Group at Morgan Stanley. He was also a Managing Director and Senior Semiconductor Analyst at Alex Brown & Sons.

Mandatory documents for ISO 17025:2017

The documents listed below are must-haves according to ISO 17025:2017. Keep in mind that if you exclude some of the clauses from the scope of your implementation, then documents for those clauses will not be required for your lab.

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Document and Record Control Procedure (Clauses 8.2.1, 8.3 & 8.4)

Quality Policy (Clauses 8.2.1 & 8.2.2)

Competence, Training and Awareness Procedure (Clause 6.2.5)

Externally Provided Products and Services Procedure (Clause 6.6.2)

Facilities and Environment Procedure (Clause 6.3)

Equipment and Calibration Procedure (Clauses 6.4.3 & 6.5)

Customer Service Procedure (Clauses 7.1.1 & 8.6)

Test and Calibration Method Procedure (Clauses 7.2.1 & 7.2.2)

Quality Assurance Procedure (Clauses 7.7.1 – 7.7.3)

Sampling Procedure (Clauses 7.3, 7.5 & 7.8.5, applicable only to laboratories that do sampling)

Handling of Laboratory Test or Calibration Items Procedure (Clause 7.4)

Complaint, Nonconformity and Corrective Action Procedure (Clauses 7.9 – 7.10 & 8.7)

Testing Report Procedure (Clauses 7.8.2 & 7.8.3, applicable to testing laboratories that write test reports)

Calibration Report and Certificate Requirements Procedure (Clauses 7.8.2 and 7.8.4, applicable to calibration laboratories that write calibration certificates)

Mandatory records for ISO 17025:2017

Records are generated to demonstrate compliance with the standard and related internal procedures and serve as evidence during audits. Here are all the required records according to ISO 17025:2017:

List of Internal and External Documents (Clauses 8.2.4 & 8.3.1)

List of Types of Records (Clause 8.4)

Registry of Records for Detention/Central Archive (Clauses 8.3.2f & 8.4.1)

Quality Objectives (Clauses 8.2.1 & 8.2.2)

Training Program (Clause 6.2.3)

Training Record and Performance Monitoring (Clause 6.2.2)

Record of Attendance (Clause 6.2.2)

Competence Approval and Authorization Record (Clauses 5.6 & 6.2.5e)

Supplier Evaluation and Approval Record (Clause 6.6.2a)

List of Approved Suppliers of Products and Services (Clause 6.6.2a)

Record of Laboratory Environmental Controls (Clause 6.3.3)

List of Laboratory Equipment (Clause 6.4.13a)

Calibrated Equipment Record (Clause 6.4.13a)

Calibration Record (Clause 6.4.13e)

Equipment Maintenance Record (Clause 6.4.13g)

Customer Order Review (Clause 7.1.1a)

Method Verification, Validation and Development Record (Clauses 7.2.1 & 7.2.2)

Sampling Plan (Clause 7.3.1) (as applicable)

Sampling Report (Clause 7.3.3) (as applicable)

Corrective Action Report (Clause 8.7.3)

Complaint, Nonconformity and Corrective Action Report Log (Clause 8.7.3)

Measurement Uncertainty Record (Clause 7.6.3)

Audit Nonconformity Report (Clause 8.8.2d)

Internal Audit Report (Clause 8.8.2e)

Management Review Record (Clause 8.9.2)

Commonly used non-mandatory ISO 17025 documents and records

You should also maintain any other documents and records that you have identified as necessary to ensure your management system can be maintained efficiently and improve over time, such as:

Addressing Risks and Opportunities Procedure (Clauses 8.5.2 & 8.5.3)

Report of Customer Satisfaction (Clause 8.6.2)

Internal Audit Procedure (Clause 8.8.2)

Management Review Procedure (Clause 8.9)

Think of the enormous benefit to you and your laboratory

You might be overwhelmed with all the documents and records listed here, but try to think in a positive way – such documents will help you organize your laboratory in a better way, and help you not to forget something that might prove to be very important.

Hurricane chris 51 50 ratchet download zip. For more help with managing the documents and all other aspects of the implementation project, download this free, easy-to-use Project Plan for ISO/IEC 17025 implementation.

About the author:

Chany Runnels has a BS in Biology and an MBA with a concentration in Organizational Management. She has consulted in healthcare, industry, and government, providing roadmaps for the implementation of Quality Management Systems. She has successfully led laboratories in the manufacturing verification of medical devices, which were distributed domestically and internationally. These devices were compliant with FDA cGMP and modeled in accordance with ISO 13485. Previously serving as a Forensic Biology SME, she has been qualified as an auditor for ISO 17025/Forensic Testing Agencies and the FBI’s QAS.

The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required to our current documents?” or “What new documents do we need to generate to ensure compliance?” The ISO 17025:2017 standard actually requires fewer documents than the 2005 revision. In this article, you’ll find a snapshot of what documents you need to have to be compliant with the 2017 revision of ISO 17025.

Mandatory documents for ISO 17025:2017

The documents listed below are must-haves according to ISO 17025:2017. Keep in mind that if you exclude some of the clauses from the scope of your implementation, then documents for those clauses will not be required for your lab.

Document and Record Control Procedure (Clauses 8.2.1, 8.3 & 8.4)

Quality Policy (Clauses 8.2.1 & 8.2.2)

Competence, Training and Awareness Procedure (Clause 6.2.5)

Externally Provided Products and Services Procedure (Clause 6.6.2)

Facilities and Environment Procedure (Clause 6.3)

Equipment and Calibration Procedure (Clauses 6.4.3 & 6.5)

Customer Service Procedure (Clauses 7.1.1 & 8.6)

Test and Calibration Method Procedure (Clauses 7.2.1 & 7.2.2)

Quality Assurance Procedure (Clauses 7.7.1 – 7.7.3)

Sampling Procedure (Clauses 7.3, 7.5 & 7.8.5, applicable only to laboratories that do sampling)

Handling of Laboratory Test or Calibration Items Procedure (Clause 7.4)

Complaint, Nonconformity and Corrective Action Procedure (Clauses 7.9 – 7.10 & 8.7)

Testing Report Procedure (Clauses 7.8.2 & 7.8.3, applicable to testing laboratories that write test reports)

Calibration Report and Certificate Requirements Procedure (Clauses 7.8.2 and 7.8.4, applicable to calibration laboratories that write calibration certificates)

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Mandatory records for ISO 17025:2017

Records are generated to demonstrate compliance with the standard and related internal procedures and serve as evidence during audits. Here are all the required records according to ISO 17025:2017:

List of Internal and External Documents (Clauses 8.2.4 & 8.3.1)

List of Types of Records (Clause 8.4)

Registry of Records for Detention/Central Archive (Clauses 8.3.2f & 8.4.1)

Quality Objectives (Clauses 8.2.1 & 8.2.2)

Training Program (Clause 6.2.3)

Training Record and Performance Monitoring (Clause 6.2.2)

Record of Attendance (Clause 6.2.2)

Competence Approval and Authorization Record (Clauses 5.6 & 6.2.5e)

Supplier Evaluation and Approval Record (Clause 6.6.2a)

List of Approved Suppliers of Products and Services (Clause 6.6.2a)

Record of Laboratory Environmental Controls (Clause 6.3.3)

List of Laboratory Equipment (Clause 6.4.13a)

Calibrated Equipment Record (Clause 6.4.13a)

Calibration Record (Clause 6.4.13e)

Equipment Maintenance Record (Clause 6.4.13g)

Customer Order Review (Clause 7.1.1a)

Method Verification, Validation and Development Record (Clauses 7.2.1 & 7.2.2)

Sampling Plan (Clause 7.3.1) (as applicable)

Sampling Report (Clause 7.3.3) (as applicable)

Corrective Action Report (Clause 8.7.3)

Complaint, Nonconformity and Corrective Action Report Log (Clause 8.7.3)

Measurement Uncertainty Record (Clause 7.6.3)

Audit Nonconformity Report (Clause 8.8.2d)

Internal Audit Report (Clause 8.8.2e)

Management Review Record (Clause 8.9.2)

Commonly used non-mandatory ISO 17025 documents and records

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You should also maintain any other documents and records that you have identified as necessary to ensure your management system can be maintained efficiently and improve over time, such as:

Addressing Risks and Opportunities Procedure (Clauses 8.5.2 & 8.5.3)

Report of Customer Satisfaction (Clause 8.6.2)

Internal Audit Procedure (Clause 8.8.2)

Management Review Procedure (Clause 8.9)

Think of the enormous benefit to you and your laboratory

You might be overwhelmed with all the documents and records listed here, but try to think in a positive way – such documents will help you organize your laboratory in a better way, and help you not to forget something that might prove to be very important.

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For more help with managing the documents and all other aspects of the implementation project, download this free, easy-to-use Project Plan for ISO/IEC 17025 implementation.

About the author:

Chany Runnels has a BS in Biology and an MBA with a concentration in Organizational Management. She has consulted in healthcare, industry, and government, providing roadmaps for the implementation of Quality Management Systems. She has successfully led laboratories in the manufacturing verification of medical devices, which were distributed domestically and internationally. These devices were compliant with FDA cGMP and modeled in accordance with ISO 13485. Previously serving as a Forensic Biology SME, she has been qualified as an auditor for ISO 17025/Forensic Testing Agencies and the FBI’s QAS.

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NABL accredited laboratory in Chennai

NABL National Accreditation Board for Testing & Calibration Laboratories (NABL) provides accreditation to Conformity Assessment Bodies (Laboratories). NABL Schemes include Accreditation (Recognition) of Technical competence of testing, calibration, medical testing laboratories, Proficiency testing providers (PTP) & Reference Material Producers (RMP) for a specific scope following ISO/IEC 17025, ISO 15189, ISO/IEC 17043 & ISO 17034:2016 Standards. It has Mutual Recognition Arrangement (MRA) with Asia Pacific Laboratory Accreditation Cooperation (APLAC), International Laboratory Accreditation Cooperation (ILAC). NABL is a constituent board of Quality Council of India which is an autonomous body setup under Department for Promotion of Industry and Internal Trade (DPIIT), Ministry of Commerce and Industry, Government of India NABL provides accreditation in all major fields of Science and Engineering such as Biological, Chemical, Electrical, Electronics, Mechanical, Fluid-Flow, Non-Destructive, Photometry, Radiological, Thermal & Forensics disciplines under testing facilities and Electro-Technical, Mechanical, Fluid Flow, Thermal, Optical & Radiological disciplines under Calibration facilities. In the field of Medical Testing laboratories accreditation is granted in Clinical Biochemistry, Clinical Pathology, Haematology & Immunohaematology, Microbiology & Serology, Histopathology, Cytopathology, Genetics, Nuclear Medicine (In-vitro tests only) disciplines. In addition, NABL offers accreditation for Proficiency testing providers & Reference Material producers for which it has APLAC MRA. Benefits of accreditation NABL is a Full member (ILAC MRA signatory) to ILAC as well as APLAC Mutual Recognition Arrangements (MRA), based on mutual evaluation and acceptance of other MRA Partner laboratory accreditation systems. Such international arrangements facilitate acceptance of test / calibration results between countries to which MRA partners represent. Read More

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Tại sao cần công nhận VILAS? Hệ thống VILAS là gì?

Nhắc đến phòng thí nghiệm, chúng ta thường nghe: được công nhận VILAS. Vậy VILAS là gì? Tại sao cần công nhận VILAS? Điều kiện nào để công nhận VILAS?

Những lĩnh vực được công nhận VILAS

Trước năm 1999, VILAS sử dụng hướng dẫn ISO/IEC Guide 25 và EN 45001 để làm chuẩn mực đánh giá. Ngày 15/12/1999, khi ISO ban hành tiêu chuẩn ISO/IEC 17025:1999, VILAS sử dụng chuẩn ISO/IEC 17025 là chuẩn để tiến hành đánh giá công nhận năng lực của các phòng thử nghiệm, hiệu chuẩn. Đến nay, chuẩn ISO/IEC 17025 đã có phiên bản là ISO/IEC 17025:2017, chuẩn này cũng được tất cả các tổ chức/chương trình công nhận của các nước và quốc tế sử dụng để tiến hành đánh giá công nhận năng lực phòng thử nghiệm, hiệu chuẩn (gọi chung là phòng thí nghiệm). Vì Vậy, nếu ai đó nói về chuẩn VILAS chính là đang nói về tiêu chuẩn ISO/IEC 17025:2017.

Hiện nay có những lĩnh vực dưới đây được VILAS công nhận:

Cơ

Hóa

Sinh

Dược phẩm

Điện - Điện tử

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Trên thực tế mọi người hay nhầm chuẩn VILAS. Tuy nhiên VILAS không có chức năng đưa ra tiêu chuẩn. Đấy chỉ là những phòng thí nghiệm được VILAS công nhận phù hợp chuẩn ISO/IEC 17025:2017.

VILAS là gì?

VILAS được viết tắt từ cụm từ Vietnam Laboratory Accreditation Scheme. là một trong các hệ thống công nhận phòng thí nghiệm phù hợp tiêu chuẩn ISO/IEC 17025:2005. VILAS là một trong những chương trình công nhận của Văn phòng Công nhận Chất lượng Việt Nam (BoA - Bureau of Accreditation Vietnam, BoA là thành viên MRA của các tổ chức công nhận khu vực và Quốc tế APLAC, ILAC, tham gia các hoạt động trong các tổ chức ILAC, APLAC và PAC).

>>> Thông tin chi tiết vui lòng xem thêm tại đây: http://akme.com.vn/du-an-akme/phong-sach-nha-may-dien-tu

Vậy tại sao cần công nhận VILAS?

Phòng thí nghiệm được công nhận VILAS tức là phòng thí nghiệm đó đã được Quốc tế công nhận về năng lực và quan trọng hơn hết là kết quả các phép đo lường/thử nghiệm của các PTN đó đã được Nhà nước thừa nhận về tính pháp lý. Điều này được khẳng định tại Điều 16 Chương III trong Nghị định 179/2004/NĐ-CP được Chính phủ ban hành vào ngày 21/10/2004.

Một phòng thí nghiệm muốn tồn tại và phát triển trong tương lại, thì việc được công nhận phòng thí nghiệm đó phù hợp với tiêu chuẩn quốc tế ISO/IEC 17025:2017 là một yêu cầu bắt buộc

Ý nghĩa thương mại : Kết quả thử nghiệm tại các phòng thí nghiệm đạt chuẩn VILASgóp phần giảm thiểu các hàng rào kĩ thuật trong thương mại; tránh việc thử nghiệm/chứng nhận lặp lại nhằm tiết kiệm thời gian và chi phí cho doanh nghiệp.

Đơn vị thi công phòng Thí nghiệm uy tín tại Hà Nội

Công ty TNHH Thương Mại và Kỹ Thuật Anh Khang là một trong những đơn vị hàng đầu về thiết kế và thi công phòng sạch tại Hà Nội. Anh Khang ME chuyên thi công các hạng mục liên quan đến lĩnh vực phòng sạch. Chúng tôi có hơn 10 năm kinh nghiệm xây dựng phòng sạch cho các lĩnh vực:

Phòng sạch Thực phẩm

Phòng sạch Dược phẩm

Phòng sạch Mỹ phẩm

Phòng thí nghiệm

Phòng mổ

Phòng sạch điện tử

Trải qua một thời gian dài tích lũy, Anh Khang ME được nhiều đơn vị lớn nhỏ trong nước chọn làm nhà thầu thiết kế và thi công phòng sạch.

Thông tin chi tiết về TƯ VẤN - THIẾT KẾ - THI CÔNG PHÒNG SẠCH, vui lòng liên hệ:

Công ty TNHH Thương mại & Kỹ thuật Anh Khang

Hotline: 1900 636 814

Email: info@akme.com.vn

Website: akme.com.vn

[4cconsulting]

NABL – ISO 17025 Accreditation: Requirements, Implementation, And Benefits For Your Laboratory

National Accreditation Board of Testing and Calibration Laboratories (NABL) gives accreditation to Conformity Assessment Bodies i.e. Laboratories. It is an autonomous body under the aegis of Department of Science and Technology, Govt. of India that is registered under the Societies Act. It has a Mutual Recognition Arrangement (MRA) with Asia Pacific Laboratory Accreditation Cooperation (APLAC) as well as International Laboratory Accreditation Cooperation (ILAC).

The objective of the NABL Establishment

The sole purpose of the NABL-ISO 17025 is to provide third-party assessment to ensure excellent quality and technical competence of testing and calibration laboratories, which enables the government and the industry to streamline and maintain the standardized quality environment.

NABL provides accreditation to laboratories in the Major Fields of Science and Engineering that are performing tests and calibrations as per ISO 17025 and ISO 15189.

Some of the few fields where NABL-ISO 17025 can be applied include Mechanical, Chemical, Electrical, Electronics, Biological, Fluid-Flow, Non-Destructive, Radiological, Thermal and Forensic, Electro-Technical, etc. Also, NABL-ISO 17025 provides accreditation to proficiency testing providers and reference material producers.

NABL-ISO 17025 Implementation Steps

NABL-ISO 17025 implementation in your existing environment can be simple and hassle-free. Also, you can choose to participate in various proficiency programs to improve your testing competencies. You can integrate new learning and updated techniques to enhance the quality of results in your laboratories. In order to remain NABL-ISO 17025 compliant and maintain accreditation, you must also get a periodical re-evaluation done by the accreditation body. To avail of the numerous benefits of NABL-ISO 17025 accreditation, follow the essential steps while implementing NABL 17025 in your existing environment.

Appoint a project manager/owner.

Define the Scope for Certification.

Research and understand the requirements associated with the standard.

Perform a gap analysis and identify weak areas.

Prepare an action plan as per the analysis.

Consider all the information and standard requirements to prepare action plans.

Proceed ahead with the action plan.

Benefits of NABL-ISO 17025 accreditation

NABL-ISO 17025 accreditation has several types of benefits including internal as well as external. The majority of the practical benefits can be witnessed on your day-to-day operation in the laboratory which also enables you to improve testing competency, streamlined management, lessened challenges or glitches, and improved results. Eventually, the growing benefits of NABL-ISO 17025 accreditation can help you with not only financial benefits but also recognize you for accuracy and details. Some of the key benefits of NABL-ISO 17025 accreditation are explained below.

[ninjanews]

What is Calibration?

Calibration is a comparative process where a known value of a standard instrument with higher accuracy is applied to a device under calibration (DUC) and the corresponding output readings are recorded under certain conditions of the DUC.

 It should be kept in mind that calibration is not only related to the conduct of comparison, but also to the resulting adjustment. The calibration unveils a new certificate of measurement uncertainty. Uncertainty is a statistical scraper of values calculated as the result of a measurement that reflects incomplete knowledge of quantitative values.

 For the evaluation and identification of issues related to calibration devices that affect the accuracy of operations and for this reason calibration is carried out.

Calibration with Traceability

The property of the measurement results can be related to the appropriate values through a comparatively unbroken chain that is referred to as traceability.

 All calibrations should be implemented as identifiable as international or unit, nationally or internationally accepted standards such as SI. 

In order to maintain the initial standard of measurement, there is the National Meteorological Institute (NMI) which supports the metrological infrastructure of the country from level to level of tree processing.

 Examples of NMI are NIST in USA, NPL in UK, PTB in Germany.

Below is a real-time example to understand the traceability pyramid from below to choose the level:

Consider, you have a lot of processing like transmitters in your plant

The process instrument is then regularly calibrated by the process calibrator to determine your functional value.

The process calibrator will then send your external / internal maximum reference standard lab to your plant.

After that, most reference standards are passed to the accepted primary standard

After that, most reference standards are passed to the accepted primary standard

The primary standard lab will derive their value from these

NMIs work with international level labs and make an international difference to ensure their calibration level

International level laboratories are based on SI in their labs

From the traceability pyramid, it has been observed that the functional value is not sorted by the primary value, which means that the executed calibration standard can search NMI through all the standards used to calibrate, no matter how many steps exist in the functional value and NMI.

 For example, U.S. customers can send their instruments directly to NIST before calibrating from another calibration lab, although this is an expensive task.

Typically, the functional standard instrument is sent to a standard lab that has more accurate testing instruments.

When moving along the pyramid, it is best practice to maintain a 4: 1 accuracy ratio. For example, if a customer's clamp meter AC current accuracy is 0.4% FS (full scale, FS), it should be calibrated with a better value of 0.1% FS or better.

 It is important to remember that the cost of calibration equipment and accuracy will increase to remove the pyramid.

Quality Standardization

In order to promote the quality of calibration, it is necessary to establish traceability that is satisfied by a quality difference, directly or indirectly, of national standards, international standards or certified reference elements. 

It can be acquired by the Government BSTI (Bangladesh Standards and Testing Institute) National Level Laboratory-run by the National Government or by non-governmental organizations.

The quality management system provides an effective metrology system that combines all measurement tools with systematic, repetitive and documented calibration.

 To meet this traceable function ISO 9000 and ISO 17025 need to determine how to quantify them.

In order to achieve the quality of calibration service, a defined confidence level exploratory uncertainty statement is often combined with calibration standards. Measuring devices and instruments according to physical quantity varies internationally such as NIST 150-2G in the US, NABL-141 in India.

 Uses two standards that cover different materials that measure different physical quantities e.g. electrical parameters (voltage, current, resistance, power, frequency, capacitance, inductance), mechanical quantities (pressure gauge, vacuum gauge, pressure switch, limit switch, trans.

 Deadweight tester pressure gauge / pressure switch for various test devices used for different test devices such as, equilibrium), thermal properties (temperature switch, temperature controller, temperature controller), noise, light, vibration, time, electromagnetic radiation and ionization radiation etc.

 Used for calibration, IR (infrared) calibrator is performed for non-contact temperature measuring device calibration and multiproduct calibration is used for calibration of electrical equipment.

How calibration relates to revenue?

From Figure 20 above we noticed that inside the process vessel there is process fluid which is burned by the burner. And there are two transmitters - pressure and temperature transmitters.

The pressure transmitter connects to the pressure indicator (PLC controlled) through a 24V loop supply. The process measures the pressure of the fluid, providing information to the pressure indicator by the pressure transmitter 4-20 mA loop current.

Suppose, the pressure index manages 0-300 psi; When the pressure transmitter delivers 4 mA, the pressure indicator shows 0 psi; When the pressure transmitter gives 20 mA, the indicator shows 300 psi. And according to the PLC output, the pressure valve will open or close.

And for the same executive for the temperature issue. By sensing the temperature inside the container through the temperature sensor, the temperature transmitter provides information to the temperature indicator by a 4-20 mA loop current.

 Depending on the temperature indicator output the flow control valve can open or close and control the flow of natural gas.

Thus, if an error occurs in the measurement of temperature or pressure in a material, an error in fuel control, then an inefficient use of the fuel, ultimately leads to a huge gross loss in production.

 This is why you need to calibrate all your materials periodically to prevent your annual loss or increase your income.

Calibration Services in Bangladesh

Prior to the commencement of calibration services, qualification demonstrations and risk assessments and its management-approval are required to verify compliance with standards and regulations.

 Each country has accreditation bodies like BAB (Bangladesh Accreditation Body) in Bangladesh, NABL for India. BAB is the national authorized body, which is responsible for the recognition of Bangladesh and maintains the Appalachian / ILAC MRA status in accordance with international norms.

Sadly for many of us - if we calibrate our external equipment from outside Bangladesh, it will be more valuable; This is a completely wrong idea. This misconception is first of all a waste of money as well as time-saving work tasks. 

Since there are so far 10 approved calibration laboratories in Bangladesh in various fields such as mechanical, thermal, electrotechnical, why is it necessary to go outside Bangladesh? If we calibrate from our internal resources, it will reduce our equipment downtime as a result of our foreign exchange.

[lonnysapotheek]

Can you trust Turkey-approved Alipza? Is it the same as U.S.-Approved Livalo?

This post is mostly a story about a very well manufactured, safe and effective, foreign version of an FDA-approved drug. These drugs are normally far less expensive than the FDA-approved version sold in the U.S. and arguably just as safe. The FDA can prevent the importation of such drugs – but the agency is actually encouraged by law not to do so if the import is for personal use only. It’s also a story about consumers and their providers navigating conflicting public information about buying less expensive medicines online from foreign countries.

A friend of mine, who has very difficult to control cholesterol, was prescribed Livalo, an FDA-approved brand of the drug pitavastatin. Let’s call him John. With his insurance, Livalo still costs John about $310 for a three-month supply – about 90 pills. He doesn’t want to pay that much if he can help it. John knows about our company, PharmacyChecker. He went to our site to discover that brand-name Livalo (pitavastatin) costs only $90 for a three-month supply at the lowest-cost PharmacyChecker-accredited international online pharmacy: a savings of 71%. That wasn’t enough to convince John to move forward with the purchase. Why not? That brand-name pitavastatin, sold in Turkey, is sold under the name Alipza – not Livalo.

John’s doctor was skeptical of drugs bought online from other countries. Is the drug safe? Is it counterfeit? Is it really the same? We know there are many doctors, nurses and other prescribing medical professionals who recommend PharmacyChecker or have learned of trusted licensed foreign pharmacies though their own research. Other medical professionals, however, are subject to the same scare tactics as consumers, ones perpetrated by drug company-funded organizations. In fact, medical professionals are targeted by such groups’ education programs. For example, the Alliance for Safe Online Pharmacies, which has received lots of money from drug companies, and the Federation of State Medical Boards teamed up to offer a “continuing education program” for pharmacists and physicians. The stated goal is to teach them: “What Providers Need To Know.” The gist is to inform them that 1) buying drugs on the Internet can be dangerous; and 2) the only way to stay safe is by sticking to U.S. pharmacies.

So, John was skeptical, even though he knows what we do at PharmacyChecker, which is accrediting only the safest international online pharmacies. In fact, when I heard about the price differentials, I became skeptical, too – but in a different sense. I know the medicines sold by PharmacyChecker-accredited online pharmacies are lawfully-manufactured, safe and effective drugs. That was not my concern. John wanted to know if these prices were for the “same” drug. That word “same” is hard to answer when it comes to prescription drugs. For example, when I’m asked if an FDA-approved generic is the exact same as the FDA-approved brand, my answer is often “no.” That response is related to well-made generic drugs – not those discovered as inferior due to fraud or poor manufacturing, which is a serious problem. The generic may very well work the same way as the brand, but it almost always looks different, comes in different packaging, and, while the active pharmaceutical ingredient is the same, inactive ingredients are usually different. And that’s in the same country.

Approved drugs with the same active pharmaceutical ingredients but sold in different countries are often not the exact same. Sometimes they are. Sometimes they are not. This includes brand-name drugs created by the same pharmaceutical company. The exact same FDA-approved drugs are sold in America and other countries, but with different labels. In many other cases, there are foreign versions of FDA-approved drugs sold by the same drug companies.

What do I tell John?

The retail price of 90 pills of Livalo without insurance is about $1,000 (far more than John pays with his insurance: about $310). That would make it over 10 times more expensive than the $90 brand Alipza. That made me consider the possibility that there was an error on our site, and we were showing the generic version price, which is available in India. After some research we found out that it is really the brand, Alipza not Livalo. Alipza is the name for branded pitavastatin in many European countries and in Turkey. The drug company responsible for marketing both Livalo and Alipza is called Kowa Pharmaceuticals, a Japanese company.

So, are these the “same” drug?

I believe the answer is an unequivocal yes: Livalo and Alipza are the exact same.

They have the exact same active ingredient, pitavastatin – and appear to have the exact same inactive ingredients. They were both approved by the world’s top regulatory authorities for safety and efficacy: Livalo by the U.S. FDA and Alipza by the United Kingdom Medical and Health Product Regulatory Authority. Interestingly, MHRA approved the marketing of Kowa’s pitavastatin under both Livalo and Alipza in the application’s approval.

Here’s a difference between Livalo and Alipza besides the name

Livalo, sold in the U.S., is made in Japan or Ohio. The Alipza is licensed to Italian drug company Recordati and manufactured in France by Pierre Fabre Médicament Production. Should that cause concern? No. France, according to the FDA, is recognized as having similarly strict pharmaceutical regulations to the U.S., per a mutual recognition agreement (MRA) signed in 2017. Not that this MRA is necessary for us to have confidence in France’s regulatory capabilities, meaning the FDA’s counterpart, called The French National Agency for Medicines and Health Products Safety, was known to properly regulate drug manufacturing before the MRA. The MRA is more proof that the FDA’s position is that drugs manufactured in France can meet U.S. requirements. According to the FDA:

“Under the Food and Drug Administration Safety and Innovation Act, enacted in 2012, FDA has the authority to enter into agreements to recognize drug inspections conducted by foreign regulatory authorities if the FDA determined those authorities are capable of conducting inspections that met U.S. requirements.”

But we can drill down further here. The French drug manufacturing company itself is registered directly with the U.S. FDA: PIERRE FABRE MEDICAMENT PRODUCTION. This is the company that makes the Alipza, which has the exact same active ingredient and inactive ingredients as Livalo. The Alipza sold in Turkey is manufactured by that same FDA-registered company – Pierre Fabre Medicament Production – under license Recordati Ilac Sanayi ve Ticaret A.S.

It is the same Alipza that John was looking at: available for $90 for a three-month supply, over 90% less than Livalo’s price for uninsured Americans, 70% less for insured Americans like John.

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[hailongjsc-blog]

NAM DƯỢC HẢI LONG : gia công mỹ phẩm tiêu chuẩn an toàn – đạt tiêu chuẩn CGMP-ASEAN- đạt tiêu chuẩn ILAC-MRA (Hoa Kỳ)

[viletto]

ASKİ laboratuvarına uluslararası akreditasyon

ASKİ laboratuvarına uluslararası akreditasyon

Yapılan akreditasyon denetiminden başarıyla geçen ASKİ İçme Suyu Analiz Laboratuvarı, 1 Temmuz 2020 tarihi itibarıyla TÜRKAK web sitesinde akredite edilmiş analiz laboratuar listesinde yayımlandı. Böylelikle ASKİ laboratuvarı, ILAC-MRA ve TÜRKAK akreditasyon markasından oluşan birleşik markayı kullanarak rapor düzenleme yetkisine sahip oldu. Bu raporlama yetkisiyle, yapılan içme suyu…

[iqc-tw]

via iQC 商品安全資料庫

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DNA Test Cost in Mumbai Maharashtra

New Post has been published on https://www.getbookmarking.com/story/dna-test-cost-in-mumbai-maharashtra/

DNA Test Cost in Mumbai Maharashtra

Get DNA Test Cost in Mumbai Maharashtra at the best cost. Our lab is NABL-certified, ILAC/MRA and ISO 15189:2012 accredited and offers 100% accurate results, for more details call us at +91-8010177771.