Medical Device Verification & Validation (V&V) Essentials

Verification and Validation (V&V) for Medical Devices

A professional, practice-oriented course that provides a clear and solid foundation for understanding, planning and implementing Verification and Validation activities as an integral part of medical device product development and the Quality Management System.

The course combines theory, practical examples and professional discussion.

Course Details

Duration: 2 days
Dates: 09.11.2026 and 12.11.2026
Hours: 09:30–15:30
Format: Online

What You Will Learn

Verification and Validation are the structured framework that connects the product’s intended use, design, risk controls, performance and safety.

The course provides clarity, structure and consistency in:

• The distinctions between Verification, Validation and Qualification

• The differences between design validation and process validation

• The connection between User Needs, Design Inputs, Risk Management and testing

• Integrating V&V planning into the development process

Who Should Attend?

• Medical device R&D engineers

• QA and RA professionals

• Verification and test engineers

• Professionals responsible for planning, executing, reviewing or approving V&V activities

Prerequisites

• Basic understanding of medical device design, development and the product lifecycle

• Basic understanding of risk management concepts