FDA 101 for Medical Devices
Registrar Corp's webinar provides industry with important information regarding U.S. FDA regulation of medical devices, including:
- Annual Registration Renewal
- eMDR Requirements for Adverse Events
- Unique Device Identifier (UDI) Requirements
Видео FDA 101 for Medical Devices канала Registrar Corp
- Annual Registration Renewal
- eMDR Requirements for Adverse Events
- Unique Device Identifier (UDI) Requirements
Видео FDA 101 for Medical Devices канала Registrar Corp
Показать
Комментарии отсутствуют
Информация о видео
Другие видео канала
Harvard i-lab | Understanding Medical Device DevelopmentNew U.S. FDA Food Labeling RulesDesign Controls - Requirements for Medical Device DevelopersHow to Prepare a Medical Device 510k Submission for FDA | Rob Packard | Joe HageThe FDA Drug Development Process: GLP, GMP and GCP RegulationsU.S. FDA's Unique Device Identifier (UDI) RequirementsDeveloping Biocompatibility for Medical Devices - Audrey TurleyQuality Systems RegulationsHow to Export Food to USAWhat is ISO 13485 for medical devices?Transitioning from the Medical Device Directives (MDD) to the Medical Device Regulation (MDR)What is Post Marketing Surveillance for Medical Devices? (MDR 2017/745)How to Prepare for an FDA InspectionWhat is the EU Medical Devices Regulation (MDR)?Design Control for Medical Devices - Online introductory courseThe 5 most relevant changes the Medical Device Regulation MDR introduces, that you must knowMedical Device Regulations / FDA ApprovalWhat it takes to build a $100M Medical Device Product or CompanyMedical Device Software Development Short CourseHow to register a Medical Device with FDA? (510k, PMA, de Novo...)