Видео ютуба по тегу Device Manufacturer Obligations

UDI requirements for medical device manufacturers in the EU
UDI requirements for medical device manufacturers in the EU
Webinar // UKCA Requirements for Medical Device Manufacturers
Webinar // UKCA Requirements for Medical Device Manufacturers
Краткий курс по Регламенту ЕС 2017/745 о медицинских изделиях
Краткий курс по Регламенту ЕС 2017/745 о медицинских изделиях
Medical Devices Regulation Training
Medical Devices Regulation Training
Overview of the Quality System Regulation
Overview of the Quality System Regulation
Medical Devices Regulations Webinar - 24 January 2023
Medical Devices Regulations Webinar - 24 January 2023
Post-Market Surveillance for medical device industries in the EU: responsibilities and obligations
Post-Market Surveillance for medical device industries in the EU: responsibilities and obligations
Webinar // Cybersecurity in the medical devices – How to show compliance to regulatory requirements
Webinar // Cybersecurity in the medical devices – How to show compliance to regulatory requirements
Post Market Surveillance requirements under the new European Medical Device Regulations
Post Market Surveillance requirements under the new European Medical Device Regulations
Medical Device Regulations / FDA Approval
Medical Device Regulations / FDA Approval
Introduction to U.S. FDA Medical Device Regulations
Introduction to U.S. FDA Medical Device Regulations
ISO 13485: 2016 Internal Audit Requirements l Medical Device Internal Audit l The Learning Reservoir
ISO 13485: 2016 Internal Audit Requirements l Medical Device Internal Audit l The Learning Reservoir
Medical Device Regulation, Oct. 29, 2020
Medical Device Regulation, Oct. 29, 2020
Process validation requirements for medical devices in the US and EU
Process validation requirements for medical devices in the US and EU
FDA Regulation of Medical Devices - Abridged and Simplified
FDA Regulation of Medical Devices - Abridged and Simplified