Global Handbook of Medical Devices Regulatory Affairs 2025: Navigate Global Medical Device Regulations Across 70+ Countries
The Global Handbook of Medical Devices Regulatory Affairs 2025 provides comprehensive, country-by-country insights into medical device regulations worldwide. Covering 70+ countries, it includes ...
Contract Pharma15d
The Critical Role of Regulatory Affairs in Advancing Biopharmaceutical Innovation
Exploring Regulatory Affairs, the discipline dedicated to ensuring that new drugs and biologics are safe, effective, and compliant with global standards.
Becker's Hospital Review13d
3 executives plead guilty to hiding medical device defect
Three former executives of Magellan Diagnostics, a North Billerica, Mass.-based medical device company, have pleaded guilty to charges related to concealing a malfunction in lead-testing devices that ...
Medical Device Studies, Regulatory Requirements and Adverse Event Reporting Training Course (ONLINE EVENT: May 7-8, 2025 & ON-DEMAND)
The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" has been added to ResearchAndMarkets.com's offering. This seminar provides an essential overview of ...
pharmaphorum9d
The UK market: A land of new opportunities for medical device manufacturers
Manufacturers are turning to consultancies specialising in medical device regulatory affairs for their UKRP needs, as these can typically grant access to an entire team of specialists and offer ...
Al Bawaba News1mon
A Decade of Excellence: GCC Regulatory Affairs Pharma Summit Draws 650+ Industry Leaders in Dubai
The 10th edition of the GCC Regulatory Affairs Pharma Summit ... around the regulations in the Pharmaceutical & Medical Devices industry. It is a perfect platform to gather market intelligence ...