The US Food and Drug Administration (FDA) has cited a medical device manufacturer and a contract drug testing laboratory for ...
This intensive symposium covers the 2026 pharmaceutical and medical device landscape, focusing on global supply chain integrity, GDP, and the latest GMP updates.
Outsourced medical device production offers a manufacturer the opportunity to enhance its production bandwidth, its technological capabilities, and ultimately, its profit margins. It is no surprise ...
DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...
Following the most recent revision to the EU GMP Annex1 in 2020, Eric Clement Arakel (Global Product Manager) and Myriam Gueye (Segment Marketing Manager, Applied Industries) at Sartorius will explain ...
Remaining competitive in the medical device market requires the ability to improve quality while reducing costs. Sartorius offers various solutions to improve productivity and meet rigorous compliance ...
The Ministery of Food and Drug Safety on the 3rd gave advance notice of legislation for a revision to the Enforcement Rule of the Medical Devices Act that includes introducing a "negative list" system ...
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