Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012 is a webinar that covers topics such as:
Reporting device-related deaths and serious injuries and when these are not treated as a product complaint
How will I know if I require more information about my medical device report?
Are there exemptions, variances, or alternative forms of adverse event reporting requirements?
The manufacturer`s reporting requirements and expectations
Develop, maintain, and implement written MDR procedures and achieve compliance
Learn what constitutes a MDR and how to facilitate this for compliance success
Learn why FDA is amending its MDR regulations to remove a requirement for baseline reports that the agency deems no longer necessary
Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012 brings together:
Regulatory Affairs and Compliance
QA/QC
Consultants
Engineering/Technical Services/Operations
Past Events
Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012 - 29 Nov 2012, Webinar (33506)
Important
Please, check "Managing Your Medical Device Reporting (MDR)Program for Compliance Success" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology, Pharma