LIVE WEBINAR 

Drug-Device Combination Products and Article 117

Are the regulatory complexities of Drug-Device Combination Products overwhelming you?

This webinar will explore the latest advancements and insights regarding integral Combination Products that must be registered as drugs under the current legislation. We will delve into complex topics such as:

  1. Drug Device Combination Products and article 117 
  2. How to apply for a Notified Body Opinion 
  3. Data requirements to prove compliance with the relevant general safety and performance requirements (GSPR)

Description

Did you know that MDR has amended the drug legislation regarding Combination Products?
 
Specifically, Article 117 requires manufacturers who are placing integral drug-device combination products on the market as “medicinal products” to seek a Notified Body Opinion (NBOp). 
 
Additionally, an integral drug device without CE marking needs to be registered as a pharmaceutical drug under the drug legislation. The Notified Body must also assess the conformity of the device with the relevant general safety and performance requirements (GSPR) outlined in Annex I.

What you'll learn

Speaker

Salma Michor, PhD

Salma Michor

Salma Michor is currently Division head Regulatory Affairs at the QbD Group. She served clients such as Johnson & Johnson, Novartis, Pfizer and CSL Behring. Previously, Michor worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH. 

She teaches regulatory affairs and clinical strategies at the University of Krems, Austria, and is an independent expert to the European Commission. 

Salma Michor is a member of the RAPS European Board. She holds a PhD in Bio engineering and an MSc in food and biotechnology from the University of Applied Life Sciences in Vienna, Austria; an MSc from King’s College, University of London in food technology; and an MBA from Open University and has earned the RAC (EU and Global). She is a Chartered Manager and a fellow of the Chartered Management Institute.

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