Surmodics Investigator Training for Adverse Event Reporting According to MDR
New Medical Device Regulation (MDR)Duration: Unlimited
Cost: 0 USD
SURMODICS INVESTIGATOR TRAINING FOR ADVERSE EVENT REPORTING ACCORDING TO MDR
NEW REQUIREMENTS FOR SAFETY REPORTING DURING CLINICAL INVESTIGATIONS
This course highlights new safety reporting obligations introduced by the Medical Device Regulation.
Exclusive Live Event
NEW REQUIREMENTS FOR SAFETY REPORTING DURING CLINICAL INVESTIGATIONS
This course highlights new safety reporting obligations introduced by the Medical Device Regulation.
Exclusive Live Event
