Instructor

Magdalena Wirt

Magdalena Wirt is a Clinical Development Consultant at GBA Key2Compliance, with a strong research background and expertise in IVDs. She holds a PhD in Biomedicine from Karolinska Institute and an MSc in Applied Biotechnology from Uppsala University, Sweden. With five years of industry experience, she has worked across product development, performance evaluation, and post-market surveillance, with a focus on regulatory compliance under the IVDR.

In her current role, Magdalena supports clients with medical writing, systematic literature reviews, and regulatory consulting, particularly in the areas of performance evaluation and clinical performance studies for IVD products.

Related courses to Magdalena Wirt

IVDR training series

Training series contains 3 parts, half a day each.
  1. Fundamentals of the IVDR and CE-marking of IVDs
  2. IVDR – key elements of the risk classification and technical documentation for the CE-marking process.
  3. IVDR Compliance: Demonstrating Performance and Safety for IVD Devices
Nov 18
- Dec 9, 2025
Online
IVD, IVDR

IVDR Performance Evaluation, Risk Management, incl Post-Market Surveillance and PMPF

Learn about the new rule-based risk classification. Understand how the risk classification impacts on the conformity assessment route Learn about the general safety and performance requirements and how to demonstrate compliance Understand the structure and content of the Technical Documentation Understand how design changes to the product design impact on the technical documentation
Dec 9
Online
CE-marking, IVDR, Post market, Risk

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