SPARK Europe Educational Forum: Medical Devices Regulation

SPARK Europe Educational Forum are monthly open meetings hosted by UiO:Life Science and SPARK Europe partners.

Medical device compliance is imperative to the success of every medical device company. Failing to achieve compliance will compromise the future of the product.

It is in in everyone’s best interest to produce quality medical devices, therefore this industry is heavily regulated.

But, how do you actually achieve compliance for your medical device?
 

Please register

Programme

In this SPARK Europe event, Anne-Mari H?kelien and Ingvild Gudim will provide some answers and perspectives to these questions, covering both MDR and IVDR.


Anne-Mari H?kelienImage may contain: Glasses, Forehead, Glasses, Cheek, Smile.

Anne-Mari is a Senior Adviser at The Norwegian Medicines Agency with an extensive experience from both regulatory authorities and basic cancer research. She has also worked in a cell therapy start-up. Anne-Mari holds a PhD in molecular biology from the University of Oslo.

 

 

 

Ingvild GudimImage may contain: Person, Smile, Cheek, Lip, Chin.

Ingvild is a Senior Adviser for medical devices and IVD medical devices at The Norwegian Medicines Agency. Prior to that she was working several years as  project leader and technical lead for diagnostic immunoassay development in Gentian Diagnostics ASA. Ingvild holds a PhD in biochemistry from the University of Oslo. 

 

 

Organizer

UiO:Life Science
Published Apr. 20, 2022 12:43 PM - Last modified Apr. 27, 2022 2:21 PM