How to estimate risk for a medical device according to ISO 14971:2019

How to work with medical device risk management

What is new in ISO 14971 2019

Design Controls - Requirements for Medical Device Developers

Risk management for medical devices and ISO 14971 - Online introductory course

Webinar: Risk Management in Software as a Medical Device (SaMD) Development

Think Fast, Talk Smart: Communication Techniques

Documentation Deconstructed: Understanding the Technical file

ISO 14971:2019 & TR 24971 Explained - Medical Device Risk Management

Medical Device Software Development Short Course

NIH-FDA Webinar – Best Practices for Navigating the IDE Pre-submission process with FDA

Project Management for Product Development of Medical Devices

Understanding Sequence of Events and Hazardous Situations

Medical Devices Regulation Training

DENGER LAGU NAFF GAK ADA BOSENNYA || 30 LAGU JADI INGET MASA LALU || Terendap Laraku |Kenanglah Aku

Short course on SaMD (Software as a medical device), IEC 62304 and IEC 82304-1

Six steps to ISO 13485:2016 Certification and MDSAP Certification

Developing a Testing Plan for Medical Device Design Verification

Risk control measures in medical device software

Process Validation for Medical Device Manufacturers

British Acupuncture Council: Wales Licensing Summary, October 2024