Quality Management

“Strategies for Addressing Data Management Challenges in Financial Institutions”

Source Node: https://platodata.network/platowire/strategies-for-addressing-data-management-challenges-in-financial-institutions/
Time Stamp: April 4, 2023 5:06 PM - Modified On: April 4, 2023 - Published By:
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Republished By Plato

Financial institutions are among the most data-intensive organizations in the world. They generate and process vast amounts of data on a daily basis, ranging from customer information to transactional data, market data, and regulatory information. However, managing this data can be a daunting task, especially given the complex regulatory environment and the increasing volume and variety of data. In this article, we will discuss some strategies for addressing data management challenges in financial institutions.1. Develop a Data Management StrategyThe first step in addressing data management challenges is to develop a

Overview of Thailand’s Draft Quality System Regulation

Source Node: https://zephyrnet.com/thai-draft-regulation-on-quality-system-overview/
Time Stamp: March 6, 2023 9:10 AM - Modified On: March 6, 2023 - Published By:
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Published by Plato

Thailand is currently in the process of implementing a new Quality System Regulation (QSR) to ensure the safety and efficacy of drugs and medical devices. The QSR is designed to ensure that all products meet the highest standards of quality and safety. This article will provide an overview of the QSR and its implications for the pharmaceutical and medical device industries in Thailand. The QSR is a comprehensive set of regulations that cover the entire lifecycle of pharmaceutical and medical device products, from development to manufacturing to distribution. It includes

Regulatory Strategy for Medical Device Development: An Overview of Effective Strategies

Source Node: https://zephyrnet.com/effective-regulatory-strategist-for-medical-device/
Time Stamp: March 6, 2023 6:41 AM - Modified On: March 6, 2023 - Published By:
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Published by Plato

The development of medical devices is a complex process that requires careful consideration of regulatory requirements. Regulatory strategy is an essential part of the development process and can help ensure that the device meets all applicable standards and regulations. This article will provide an overview of effective regulatory strategies for medical device development.The first step in developing a regulatory strategy is to identify the applicable regulations and standards. This includes both national and international regulations, as well as any specific requirements for the particular device. Once the applicable regulations and

How the EU Medical Device Regulation is Affecting Medical Device Innovation

Source Node: https://zephyrnet.com/is-eu-mdr-harming-medical-device-innovation/
Time Stamp: March 1, 2023 11:41 AM - Modified On: March 1, 2023 - Published By:
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Published by Plato

The European Union Medical Device Regulation (EU MDR) is a major piece of legislation that has been implemented to ensure the safety and efficacy of medical devices. This regulation has been in effect since May 2020, and it is having a significant impact on medical device innovation. The EU MDR requires medical device manufacturers to provide detailed information about their products, including clinical data, safety and performance data, and post-market surveillance data. This information must be submitted to the European Commission for review and approval. The EU MDR also requires