Events & webinars


Biocompatibility and ISO 10993 - how to evaluate the safety of your medical device
Wednesday, December 2, at 2 PM (EET)
In this expert webinar, we will dive into biocompatibility testing of medical devices. We will start from the basics of what biocompatibility means and why different devices should be evaluated differently, and then go deeper into Biological Evaluation Plans and the tests themselves.
During the 1-hour session, you will learn at least the following:
What the biological evaluation consists of, from material characterization to biological tests
How to determine what ISO 10993 tests are needed for your device
What to do if the device changes?
After the presentation there will also be time for audience questions - we hope to have a lively discussion!
Available recordings
Formaldehyde emission testing according to the new REACH requirements
Analyzing micropollutants in water: pharmaceutical residues, microplastics, and PFAS
Techniques for contamination analysis of thin films and wafers
Streamlining EU MDR approval: Using your FDA preclinical & clinical data
Bisphenol testing of food contact materials: everything you need to know
Stay ahead of the PFAS curve: overview of regulations and analytical methods (hosted together with Regartis consultants)
Stay ahead of the PFAS curve, part 2: case examples of PFAS analysis and other practical advice (hosted together with Regartis consultants)