Dublin, Jan. 03, 2020 (GLOBE NEWSWIRE) -- The "Contract Regulatory Affairs Management Market for Medical Devices, 2019-2030" report has been added to ResearchAndMarkets.com's offering. Contract ...

As the saying goes, time is money, and this statement could not be more true for the medical device industry. Each day that passes when a device is not approved for marketing is a day of revenue loss.

The evolving EU MDR and IVDR present key opportunities for companies to enhance compliance strategies, engage with notified bodies, and optimize market access. Staying informed and proactively ...

As the biopharma space gets more competitive and the days of blockbuster drugs seem further in the rearview, biopharma companies are investing in digital to find new and innovative ways to ...

The global medical device outsourcing market size is projected to reach USD 386.08 billion by 2033, growing at a CAGR of 13.29% from 2025 to 2033. The market is driven by increasing demand for medical ...

Rockville, MD, USA, Aug. 16, 2017 (GLOBE NEWSWIRE) -- The Regulatory Affairs Professionals Society (RAPS) has published the updated, 10 th edition of Fundamentals of US Regulatory Affairs, the most ...

South Korea’s medical device market is rapidly expanding, driven by technological innovations and increasing healthcare demands. As the market grows, understanding Korean medical device regulations is ...

DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...

Dublin, Sept. 24, 2025 (GLOBE NEWSWIRE) -- The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Oct 21, 2025)" training ...