#irt clinical trial solutions

[octalsoft]

What is IRT and How Does it Impact Clinical Trials? — Octalsoft

An IRT system is also known by several other names, including IVRS, IWRS, IXRS, and RTSM, but regardless of its name, the system provides a comprehensive set of capabilities for managing patient enrollment and drug supply operations throughout the clinical trial lifecycle. IRT, or Interactive Response Technology, is a technology that automates clinical trial supply management, randomization, and analytics. IRT clinical trials guarantee that participants receive the appropriate therapy at the appropriate time, allow for improved drug supply logistics tracking, and allow researchers to collect real-time data from people during the trial.

An IRT clinical trial software can assist in enhancing productivity, decrease risks, and reduce costs in clinical investigations by providing different automation. But there’s more. Read on for the top 5 areas of impact of an IRT deployed to Clinical trials.

The Advantages of Deploying IRT to Clinical Trials

Patient Enrollment, Randomization, and Blind Protection — As compared to manual techniques, using the IRT to manage enrollment and/or randomization automates the process and eliminates human error. To preserve research blinding, the system enables for complicated protocol enrollment and randomization design and rigorously controls sensitive information such as treatment arm and drug treatment assignments.

Patient Randomization

The IRT will randomly allocate patients to treatment arms in a methodical manner. There are various commonly utilized approaches, including central, subject-stratified, and/or location-stratified randomization systems. The IRT will allocate the individual to the appropriate treatment arm during the randomization visit based on the programmed randomization process. In most cases, IRT clinical trial solutions will also provide the individual with the medicine kit that corresponds to the randomized treatment arm.

To properly grasp how effectively an IRT randomizes patients in a double-blind experiment, consider how it was done before IRT was available. When an IRT is not used, each patient on the randomization list is assigned a treatment type and matching kit number. The number is sealed in an envelope with a sequential number on it. A batch of envelopes and the related kits are sent to the experimental site, where envelopes are selected in order. The patient is subsequently given the appropriate kit.

While this approach works pretty well on a small scale, it is sluggish and only works with simple randomization patterns. Also, it is susceptible to human error.

IRT manages randomization in an automated and centralized manner. It can allow complicated classification and randomization designs that manual randomization cannot. Because randomization occurs without human interaction, it decreases human error. Furthermore, as with other parts of study management, the data is saved in the system for simple tracking. The automated randomization and medication assignment method avoids the need to maintain paper envelopes or cards at the location, where unblinded information might be compromised.

2. Study Blinding

The IRT clinical study plays a crucial role in preventing unblinded trial data from being shared improperly. Maintaining the blind in blinded trials is critical to the trial’s integrity since it prevents bias in how patients are treated. Overall, the IRT functions almost as a force field, shielding unblinded information, such as treatment arm and medicine kind, from individuals who should not have access to it. Access to system functions is limited by user privileges, so only users who should have access to unblinded data in the IRT may view it.

The ideal IRT is frequently equipped with emergency unblinding capabilities. This can be configured such that Principal Investigators can unblind patients at their locations in the event of an emergency. When the site has an emergency code breach, the system quickly alerts the research team. Often, the patient who was unblinded by the site is instantly removed from the research, prohibiting the IRT from assigning any additional drugs. The IRT can also provide patients access to the Medical Safety team, which can unblind any patient at any location without interfering with their continued participation in the trial.

3. Supply Management

Individual kits in the depot and on-site are not labeled for specific patients. Instead, patients are given kits when they come for their appointments. As a result, shipments to locations only include enough stock to fulfill patient demand for a set period of time and resupplies are triggered when stockpiles reach a predetermined level. Because products are only assigned to patients when they come in for visits, this procedure increases medicine availability at the location while minimizing drug waste. Because the IRT knows what patients are at each location, their treatment arms, and the visit schedule, it can adjust the supply delivered to each site.

Controlling costs requires developing and maintaining an accurate prediction of product demand over the length of a clinical study. The IRT gives Supply Chain Managers real-time updates on patient registration and product inventories across the supply chain. This helps with budgeting, saves waste from hoarding goods, avoids stock-outs, and decreases the need for emergency steps to replace expired pharmaceuticals.

An interactive response technology in clinical trials may also keep track of product expiry dates to ensure that the patient has enough time to take the medication before it expires. It can also notify study managers when expirations are approaching. Because of their limited shelf life, medications that must be actively controlled require this notice. Probably most importantly, an IRT provides supply managers with a comprehensive picture of available supplies at the main depot, subsidiary depot, and site levels. As a result, they may change their inventory and distribution strategies to fit the current trial circumstances.

4. Inventory Management

The IRT provides a number of capabilities to manage the supply chain in a trial, from the moment supplies are packaged and distributed at the depot to medicine assignment, drug returns, and destruction. When goods are physically packaged and made available in the system, transportation to another depot or location is initiated and tracked. When the Sponsor activates an IRT site, the system sends a request to the depot for an initial supply of medicine. The depot fulfills the order and delivers it to the spot. When an order arrives at the site, personnel confirms receipt in the IRT and makes the medications accessible for patient assignment.

Patients who visit the site are given a medicine kit from the center’s inventory. An algorithm within the system is constantly checking the inventory at each station. If the inventory falls below a certain threshold, the supply engine will submit a request to the depot to provide a replenishment. Shipments are made through this closed-loop procedure to accommodate newly enrolled patients, following visits, and any needed replacement stock. Another key feature of the IRT that is sometimes neglected is the ease with which drug accountability, returns, and destruction may be accomplished. In many research, this procedure is still done manually, which is difficult and time-consuming. Sites can save time, enhance efficiency, and minimize data by switching the process electronically via the IRT.

5. Patient Tracking and Reporting

All patient and supply data contained in the IRT database is easily accessible via reports and data lookups. This gives the clinical and drug management teams real-time access to data, study parameters, and alarms. This facilitates reviewing the research as it goes and making any required changes to things like enrollment or site inventory settings to match the exact condition of the trial at any given moment.

In Summation

An IRT, in essence, enhances trial efficiency and the quality of accessible information during a trial. Sponsors, CROs, and investigators are conducting more sophisticated studies than ever before with fewer employees and fewer resources thanks to IRT systems.

An IRT solution enables sponsors to create and use the functionality they require while eliminating extraneous complications. This method aids in reducing the time it takes to launch a clinical study, allowing much-needed treatments to reach patients faster than ever before. When time is of importance, such as in the event of a worldwide pandemic, IRT devices can really be game changers by assisting effective treatments to demonstrate benefits as quickly as feasible and at a reduced cost.

Ultimately, the adoption of an IRT empowers researchers, sponsors, and study personnel with the tools and capabilities needed to effectively manage and monitor a clinical trial, leading to reliable outcomes, improved decision-making, and the advancement of evidence-based medicine. But not every IRT matches the standards of a modern clinical trial. What you need is a vetted partner like Octalsoft that can deploy a highly efficient IRT/IWRS that matches and exceeds benchmarks. Want to know more about how Octalsoft’s IRT/IWRS can turbocharge the productivity of personnel and boost the effectiveness of your clinical trial? Book a Demo with us NOW! With Octalsoft’s systems, sponsors win, investigators win and, most importantly, patients win.

[giyadesuza]

Understanding Cystic Fibrosis Symptoms: A Comprehensive Guide

Cystic Fibrosis Disease Overview:

Cystic fibrosis (CF) Disease is a genetic disease that primarily affects the respiratory and digestive systems. It is a complex and chronic condition that requires a multidisciplinary approach for diagnosis, treatment, and management. This article provides an in-depth analysis of Cystic Fibrosis, encompassing diagnostic methods, treatment options, market dynamics, regulatory framework, competitive analysis, emerging trends, clinical trial data assessment, and a concluding perspective on this challenging disease.

The Market Competitors Listed Below are Revolutionizing Healthcare with Innovative Inventions:

Diagnostic Market Players:

Blood Test-

Roche Ltd.

Sun Pharmaceuticals Industries Ltd

Cipla Limited

Thyrocare Technologies

Dr. Reddy’s Laboratory

Dr. Lal Path labs

Fortis Healthcare

Genetic Test-

IntegraGen

Abbott

AutoGenomics

Biocartis

Bio – Rad laboratories

Cepheid

Elitech Group

Imaging Test-

GE Healthcare

Radiance Imaging System

Hitachi Ltd.

Med Imaging Solutions

DiagnoTech Corporation

Siemens Healthineers

Esaote S.p.A.

Price & Market Access

Cystic Fibrosis Diagnostic Analysis:

Early diagnosis of cystic fibrosis is vital for initiating timely treatment and improving patient outcomes. The most common diagnostic tools include:

Newborn Screening: Most cases of Cystic Fibrosis are diagnosed through newborn screening programs, which detect elevated levels of immunoreactive trypsinogen (IRT) in blood samples.

Sweat Test: The gold standard for Cystic Fibrosisdiagnosis, this test measures the chloride concentration in sweat. A higher-than-normal chloride level is indicative of Cystic Fibrosis.

Genetic Testing: Genetic tests can identify mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene. More than 2,000 CFTR mutations have been identified.

Imaging: Chest X-rays and CT scans can reveal lung damage and bronchiectasis, common features of Cystic Fibrosis.

Cystic Fibrosis Treatment Analysis:

Cystic Fibrosistreatment focuses on managing the symptoms and complications, as there is no cure. Key elements of treatment include:

Airway Clearance Techniques: Physiotherapy and devices like the Flutter or the Acapella are used to help patients’ clear mucus from their airways.

Medications: Bronchodilators, antibiotics, and anti-inflammatories help manage lung infections and inflammation.

CFTR Modulators: These innovative drugs, such as Ivacaftor, Lumacaftor/Ivacaftor, and Trikafta, target specific CFTR mutations to improve lung function and reduce symptoms.

Lung Transplantation: For severe cases, lung transplantation may be considered as a last resort.

Browse More Information:

Expanding Cystic Fibrosis Disease Market:

The market for CF treatments has been expanding due to advancements in pharmaceuticals. CFTR modulators have notably improved patients' quality of life, and pharmaceutical companies continue to invest in research and development.

Regulatory Framework for Cystic Fibrosis Disease:

Regulation for CF therapies varies by region. The U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have stringent approval processes for new CF drugs to ensure safety and efficacy. This has led to a competitive environment with high-quality treatments.

Competitive Analysis:

Pharmaceutical companies such as Vertex Pharmaceuticals, AbbVie, and Genentech/Roche have been at the forefront of CF research and drug development. They have introduced groundbreaking CFTR modulator therapies that are transforming the treatment landscape. Competition remains intense as new players enter the market.

Market Trends:

Several trends are shaping the CF landscape:

Personalized Medicine: CF therapies are increasingly becoming tailored to specific CFTR mutations, resulting in more effective treatments.

Telemedicine: The use of telehealth services has surged, allowing patients to access CF care remotely.

Patient Advocacy: CF patients and organizations are playing a more active role in research and policy advocacy.

Emerging Therapies: Ongoing research is exploring innovative therapies, including gene editing techniques.

Clinical Trial Data Assessment:

Continuous clinical trials are crucial to advance CF research and therapy development. They provide essential data on the safety and efficacy of new treatments, helping refine existing therapies and discover new ones.

Conclusion:

Cystic fibrosis remains a challenging and incurable genetic disease, but significant progress has been made in improving the quality of life for affected individuals. Early diagnosis and personalized treatments are key. As the CF market continues to expand, ongoing research, innovative therapies, and patient advocacy promise a brighter future for those living with this condition. Advances in CFTR modulators and other treatments offer hope for improved outcomes and potentially even a cure in the future.

Browse Through More Genetic Diseases Research Reports

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Breaking Barriers in Duchenne Muscular Dystrophy (DMD): Hope on the Horizon

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[cathalind-blog]

[ddiclinical]

DDi's mIRT is sophisticated randomization and clinical trials supplies management solution Manage to the end-to-end, configurable randomization and trial supply management software platform IRT Tool Quickly makes decisions and change study parameters mid stream Reduce service delivery and change order costs.

[vistaarai2020]

IRT has created its footprint in the field of clinical research and has evolved drastically in such a way that it has bought a major difference in perspective of clinical trials over the decades. It faceted itself into the streams from only randomizing the subject and assigning them to a treatment group to managing the overall supplies required throughout the study through supply management.

[livemarketnews]

Risk-based Monitoring Software Market to Reach $511 million | Increasing Adoption in Clinical Trials of Asia Pacific Region

Risk Based Monitoring Software Market is experiencing a significant growth due to the factors such as the cost and time efficiency of RBM solutions, rising number of clinical trials, and increasing government funding and grants to support clinical trials. The study involved four major activities in estimating the current size for the risk-based monitoring (RBM) software market. Exhaustive secondary research was done to collect information on the market and its different subsegments. The next step was to validate these findings, assumptions, and sizing with industry experts across the value chain through primary research. Both top-down and bottom-up approaches were employed to estimate the complete market size. After that, market breakdown and data triangulation were used to estimate the market size of segments and subsegments. [137 Pages Report] The risk-based monitoring (RBM) software market is expected to reach USD 511 million by 2025 from USD 273 million in 2020, at a CAGR of 13.3%. Market Size Estimation: Both top-down and bottom-up approaches were used to estimate and validate the total size of the RBM software market. These methods were also used extensively to estimate the size of various subsegments in the market. The research methodology used to estimate the market size includes the following: 1. The key players in the industry and markets have been identified through extensive secondary research. 2. The industry’s supply chain and market size, in terms of value, have been determined through primary and secondary research processes. 3. All percentage shares, splits, and breakdowns have been determined using secondary sources and verified through primary sources. To complete the overall market engineering process and to arrive at the exact statistics of each market segment and subsegment, the data triangulation and market breakdown procedures were employed, wherever applicable. The data was triangulated by studying various factors and trends from both the demand and supply sides in the RBM software industry. Download PDF Brochure: https://www.marketsandmarkets.com/pdfdownloadNew.asp?id=102112429 Recent Development in Industry: 1. In 2018, Bioclinica (US) launched the SMART technology suite available with Medical Imaging, Electronic Data Capture (EDC), and Interactive Response Technology (IRT) combined. 2. In 2019, Veeva Systems (US), acquired Crossix Solutions (US), a provider of privacy-safe US patient data and best-in-class analytics platform to help maximize media and marketing effectiveness. 3. In 2019, Parexel International Corporation (US), partnered with Datavant (US) to enable the connection of real-world data across all clinical trials conducted by Parexel. Key Questions Answered in The Report: 1. Which segment will dominate the RBM software market in the future? 2. Which end-user segment will dominate the RBM software market in the future? 3. Emerging countries offer immense opportunities for the growth and adoption of RBM software; will this scenario continue in the coming five years? 4. Where will all the advancements in technology offered by various companies take the industry in the mid- to long-term? 5. What are the upcoming products in the RBM software market? RBM Software Market Dynamics: Market Drivers 1. Increased outsourcing of clinical trial processes to CROs 2. Cost and time efficiency of RBM solutions 3. Increasing government funding and grants to support clinical trials 4. Increased pharmaceutical R&D spending 5. Initiatives to boost digital health to propel market growth Request Sample Report: https://www.marketsandmarkets.com/requestsampleNew.asp?id=102112429 Key Players: Oracle (US), Medidata Solutions (US), and Parexel (US). Other prominent players in the market are Bioclinica (US), Bio-Optronics (US), IBM Corporation (US), DATATRAK (US), Veeva Systems (US), DSG (US), MasterControl (US), ERT (US), Forte Research Systems (US), MedNet Solutions (US), ArisGlobal (US), Anju Software (US), MaxisIT (US), Techsol Corporation (US), OpenClinica (US), CRF Health (US), and Covance (US).

[pharmaphorumuk]

IRT Europe Summit

New clinical trial regulations are requiring sponsors to keep tighter oversight than ever before – from audit trails to tracking system changes – resulting in high costs and trial delays. IRT Europe explores implementation best practices and how interactive response technologies can be utilised to improve supply chain planning and optimise clinical trials. Take this opportunity to share and discuss current industry needs, the latest tools and solutions for forecasting and the various regulatory requirements for IRT, among many other critical topics. Register at www.cbinet.com/IRTEU.

The post IRT Europe Summit appeared first on Pharmaphorum.

from Pharmaphorum https://pharmaphorum.com/events/irt-europe-summit/

[globyzbiopharmaservice-blog]

Clinical Trial Supplies and Its Various Attributes

Successful clinical trial supplies optimization is vital and certainly, people spend too much time trying to make forecasts 100% precise. Once a project starts, it is very unusual for the real to look like the prediction?

People spend hours in a hopeless challenge to produce the faultless estimation only to result in the right forecast altered again the next week and so on. It is clear that people need some intensity of estimation in order to manage supplies but should this prediction be at a top more common level with an improved focus on the capability to respond to transforms. For example when setting up the IVRS or IRT systems for research and requesting quotes from possible vendors, how many of them actually assess the rate and time of potential changes? It is impossible to anticipate the modifications required, therefore how can you be expected to calculate the price and time of something that is unknown? Whilst the literal changes required may not be observable at the initial stage of a medical study there is no reason why you cannot work with your vendors to make system and clinical supply chain design as flexible as probable. Numerous IRT or IVRS vendors have now established advanced systems that can reply faster and run more economically to changes required whilst the arrangement is live. Some other areas that should be taken into consideration when designing flexibility into supply chains are kit designing and Clinical labeling. Clinical Supply kits should be designed to give the utmost flexibility to allow for astonishing adjustments are dosage or visit frequency. Do you regularly consider which countries are likely to be added as emergencies if enrollment doesn't go as intended and if these are known are country requirements and languages for dependent areas included in the pamphlet label from the start? There are numerous models, clinical trial supplies optimization, and forecasting devices available on the internet. They are designed to make the procedure more exact and to a level, they possibly do add some value. However, as the fact going in is usually based on the greatest guess and assumptions it is indispensable that the estimation coming out, whilst development on the customary spreadsheet or paper-based approach, will never be 100% perfect. Globyz Biopharma Services is a renowned name for sourcing and supply of commercial medicines or comparators for clinical trial studies across all therapeutic regions. It is the utmost destination for global sourcing, GMP-compliant storage, Clinical Packaging, clinical distribution, clinical labeling, and cold-chain supply solutions. Whether you need commercial medicine sourcing or complete clinical supply services including attaining, packaging and labeling, storage, and distribution or regulatory consulting, you have customized and optimal solutions tailored to your clinical trial needs as a flawless expansion of your supply chain. The company has years of experience and possesses outstanding expertise in managing the legal issues, planning, and supply chain challenges of sourcing, storing, and distributing pharmaceuticals for clinical trials. Globyz Biopharma Services is focused to provide customized solutions with the uppermost level of quality and service to make the name just perfect for comparator sourcing and supply partner for the customer’s clinical trial material necessities and services. to know more about the company and its work and services, visit the website.

[hareposto65-blog]

Consider PharMakeable for Best Supply Chain Consulting

(April 14, 2019) - PharMakeable is a supply chain consulting firm which gives a solution to different customers worldwide. The main objective of the company is its success if its customers. It implements process optimization, best operational objectives to help the business.

The company stands as a responsible firm to provide services to reduce costs of, maximize profit and increase the efficiency of firms.

The various service provides by the company are:

1. Clinical Trail Packages The company offers services for a successful clinical trial as packages. It includes paling the quantities to produce, localize relevant CROs, central labs, IRT, equipment’s, etc. They also negotiate well with the vendors to find relevant distribution centers.

2. Logistics Various kinds of shipment is offered by PharMakeable. It includes pharmaceuticals logistics, life science logistics, etc.

3. Purchasing They offer vast experience in procurement services from small to the big contract of chemicals, electronic parts, lab equipment, machinery, etc.

4. Planning and risk management They believe in accurate planning for operational excellence. The services include inventory planning, supply planning, building BOM and analyzing purchase, etc.

About The company: PharMareable is a supply chain consulting form associated with providing the best quality services to its customers. The company is successfully running to provide customers from different domains and help the business in many ways.

For more information, please visit http://www.pharmakeable.com/

Media Contact: PharMakeable Website: https://www.pharmakeable.com Email- enash@pharmakeable.com

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[octalsoft]

IWRS/IRT/RTSM: Are they different or the same?

In the world of clinical trials and research, acronyms abound, often leaving newcomers and even seasoned professionals scratching their heads. Among the confounding cluster of letters, IWRS, IRT, and RTSM stand out as crucial components of clinical trial management. But are they distinct entities, or are they simply different names for the same thing? In this blog post, we'll shine a light on these terms, unraveling their distinct roles and shedding light on the crucial differences that set them apart in the world of clinical trial management.

Understanding the Basics

IWRS - Interactive Web Response System

The interactive web response system for clinical trials or IWRS in clinical trials is a web-based tool designed to facilitate the randomization and drug supply management in clinical trials. Its primary function is to allocate subjects to different treatment groups in a randomized and controlled manner. Essentially, IWRS helps maintain the integrity and validity of clinical trial results by ensuring that the allocation of participants is unbiased.

IWRS, or Interactive Web Response System, serves as the linchpin in the randomization process of clinical trials. Picture it as the conductor orchestrating the allocation of participants to different treatment arms, ensuring a fair and unbiased distribution. It's the digital brain behind the scenes, managing the randomness that underpins the scientific validity of clinical trial results.

IRT - Interactive Response Technology

On the surface, Interactive Response Technology (IRT) may sound similar to IWRS, and indeed, the terms are often used interchangeably. However, IRT is a broader category that encompasses various technologies used to enhance the efficiency of clinical trial supply management. This includes not only randomization (as in IWRS) but also drug accountability, patient compliance tracking, and other interactive features that streamline trial operations.

While IWRS is a subset of IRT, the term IRT is broader in scope. Interactive Response Technology encompasses a suite of tools and technologies designed to enhance the efficiency of clinical trial supply management. This includes not only randomization but also features like drug accountability, patient compliance tracking, and various interactive elements that contribute to a more streamlined trial process.

RTSM - Randomization and Trial Supply Management

Randomization and Trial Supply Management (RTSM) is an umbrella term that combines both IWRS and IRT functionalities. In essence, RTSM refers to the comprehensive system that handles the entire process, from randomizing participants to managing the supply of investigational products. While IWRS randomization technology and IRT focus on specific aspects of this process, RTSM encapsulates the broader scope, emphasizing the integration of these technologies for seamless trial management.

RTSM, or Randomization and Trial Supply Management, is a comprehensive solution that merges the functionalities of IWRS and IRT. RTSM goes beyond mere randomization, incorporating a holistic approach to managing the entire lifecycle of investigational products in a clinical trial. It's the nexus where randomization, drug supply management, and various interactive technologies converge to create a unified system for seamless trial execution.

Key Differences

IWRS systems for clinical trials are a specialized system solely dedicated to randomization.

IRT is the broader category encompassing a range of interactive technologies, including randomization, drug accountability, and patient compliance tracking.

RTSM represents the all-encompassing solution that integrates IWRS and IRT functionalities, providing a comprehensive approach to randomization and trial supply management.

Conclusion

In conclusion, while the acronyms IWRS, IRT, and RTSM may seem interchangeable at first glance, they represent distinct components in the complex world of clinical trial management. Understanding their specific roles and functionalities is crucial for researchers, sponsors, and other stakeholders to ensure the smooth and successful execution of clinical trials. So, the next time you encounter these acronyms, you can confidently decipher their meanings and appreciate the intricacies of each component in advancing medical research.

[swapnamakro]

clinical trial supply management and IRT Solutions

Streamline your clinical supply management with our comprehensive solutions. Ensure efficient tracking, distribution, and optimization of trial supplies

[coolluminaryland-blog1]

E-Clinical Trial Solutions Market Size,Status and Forecast 2019

E-clinical trial solutions are a combination of technology, products and services that work together to automate and manage clinical trials. This term is used to refer to electronic systems that are used for conducting or automating the management of clinical trials and minimizing human errors.Conducting clinical trials for a novel drug requires efficient management of large amount of essential data with real-time analysis.Such management solutions improve efficiency, enhance the speed of clinical trials process, reduce clinical trial costs, and enable better data management and integration of different trial data for efficient observation.

Read Report Overview: https://www.transparencymarketresearch.com/e-clinical-trial-solutions.html

E-clinical trial solutions market is segmented on the basis of technologies employed such as clinical trials management systemsCTMS, electronic data capture (EDC) solutions, randomization and trial supply management system,electronic patient reported outcome (ePRO),interactive voice response systems (IVRS)and interactive response technology (IRT).These technologies are widely used in e-clinical trials solution systems. Similarly, geographically this market is segmented into North America, Europe, Asia-Pacific and rest of the world (RoW).This market can be further segmented on basis of the end-users, namely, healthcare providers, clinical research organizations (CROs) and pharmaceutical companies. Increasing trend in outsourcing of clinical trial processes to CROs by pharmaceutical companieshas led to an increase in the number of CROs globally. China and India are the major destinations for clinical trial outsourcing due to availability of highly skilled labor force at lower cost and overall low cost of operations. Also, on the basis of the delivery mode the global e-clinical trial solutions market can be categorized into web hosted (on-demand), licensed enterprise (on premise) and cloud-based markets.The major factors responsible for driving the growth of this market include technological advances in the field of e-clinical solutions, globalization of clinical trials and various benefits such as reduced cost of trials and increased efficiency and accuracy offered by e-clinical solutions. In the future, better, user-friendly access of software and awareness of compliance benefits will aid in increasing the acceptance and penetration of e-clinical solutions in the global market.

Request Brochure of Report: https://www.transparencymarketresearch.com/sample/sample.php?flag=B&rep_id=1792

Some of the key players operating in this market include Oracle Health Sciences, BioClinica, eResearch Technology, Inc., Clinipace Worldwide,SAS Institute, Inc., MedidataSolutions, Datatrak International, Inc.and ParexelInternational Corporation.

About us:

Transparency Market Research (TMR) is a U.S.-based provider of syndicated research, customized research, and consulting services. TMR’s global and regional market intelligence coverage includes industries such as pharmaceutical, chemicals and materials, technology and media, food and beverages, and consumer goods, among others. Each TMR research report provides clients with a 360-degree view of the market with statistical forecasts, competitive landscape, detailed segmentation, key trends, and strategic recommendations.

Contact us:

Transparency Market Research 90 State Street, Suite 700, Albany NY – 12207 United States Tel: +1-518-618-1030 USA – Canada Toll Free 866-552-3453 Email: sales@transparencymarketresearch.com Website: http://www.transparencymarketresearch.com/

[jforcs-blog]

Almac Clinical Technologies Releases New Podcast Series Entitled “Spotlight on IRT: Best Practices”

Almac Clinical Technologies Releases New Podcast Series Entitled “Spotlight on IRT: Best Practices”

Almac Clinical Technologies, a global leader in technology-enabled solutions for managing clinical trial patient and supplies data through its flagship IXRS® 3 Interactive Response Technology (IRT) debuts a first-in-industry podcast series entitled, “Spotlight on IRT: Best Practices.” This podcast features both Almac thought leaders and outside experts discussing best practices relating to IRT,…

[ddiclinical]

IRT has created its footprint in the field of clinical research and has evolved drastically in such a way that it has bought a major difference in perspective of clinical trials over the decades. It faceted itself into the streams from only randomizing the subject and assigning them to a treatment group to managing the overall supplies required throughout the study through supply management.

[hellopinksoulstudent]

During clinical trials, randomization and trial supply management (RTSM) solutions help randomize the participant allocation and make sure the study design is balanced and trial supplies are available when and where they are required. A key piece of those efforts is the usage of interactive response technology (IRT) software.