Draft amendments to the Medical Device Rules seek to reduce manufacturing licence timelines for Class B, C and D devices to ...
The Union health ministry has notified an amendment to the Medical Device Rules (MDR), 2017, to incorporate the qualifications required for the recruitment of inspectors and government analysts for ...
Kathy Murray - McDermott International, Inc. David Dickson - McDermott International, Inc. Stuart A. Spence - McDermott International, Inc. Good day, ladies and gentlemen and welcome to the McDermott ...
Health ministry proposes amendments to MDR, 2017 to streamline licensing process: Our Bureau, New Delhi Monday, June 29, 2026, 12:30 Hrs [IST] The ministry of health and family we ...
LE MONT-SUR LAUSANNE, Switzerland--(BUSINESS WIRE)--Regen Lab, a global commercial-stage medical technology company specializing in the research, development, registration, manufacturing and ...
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" ...
InGeneron, Inc., a biotechnology company pioneering autologous regenerative cell therapies, today announced receipt of a CE Certificate (No. 28620235524 issued January 19, 2026) for the Transpose ...
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