According to a comprehensive market research report titled "Medical Device Contract Manufacturing Market Size, Share, ...

Dublin, June 30, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" training has been added to ResearchAndMarkets.com's offering ...

Received Medical Device Regulatory Approval in April 2022 NASH (Nonalcoholic steato-hepatitis) App currently in development and undergoing clinical trials with the University of Tokyo Hospital ...

Company Logo. The Global Handbook of Medical Devices Regulatory Affairs 2025 provides comprehensive, country-by-country insights into medical device regulations worldwide. Covering 70+ countries, it ...

Please use one of the following formats to cite this article in your essay, paper or report: APA. DSI, a PLG Company. (2024, July 11). Regulatory strategy for medical devices approval.

These two regulations involve a wide-range of measures, including securing medical device-related documentation requirements, monitoring devices, and restricting and reporting substances used in ...

Artificial intelligence (AI) is no longer the future of healthcare—it’s already here. AI-driven medical devices are diagnosing diseases faster than doctors, guiding surgical procedures with ...

The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has put out a call for developers of artificial intelligence as a medical device (AIaMD) technology to join its new regulatory ...

India's regulatory body for drugs has now become an affiliate of the International Medical Device Regulators Forum. About Careers Internship MedBlog Contact us English (US) ...