MD&M West 2021 Tech Talk presentation

10th August 2021

Eric Uffman, Sales director, EAG Laboratories presented Chemical Characterization for MDR Compliance calls at MD&M West 2021 Tech Talk. On May 26th of this year, the new Medical Device Regulation (“MDR”) went into effect for devices marketed in Europe. This regulation calls out over 1,000 substances that are “carcinogenic, mutagenic or toxic to reproduction (‘CMR’)” and requires that these substances cannot be present at more than 0.1% (by wt.) in a medical device. EAG has developed an evaluation program that combines a systematic review of material data and application use along with chemical screening and evaluation against the MDR standard.  We will discuss this time and money saving approach and how this testing compares with ISO 10993-18 testing.

Chemical Compatibility

More content you might like...

RBS

RBS Webinar

In this webinar we will focus on Rutherford Backscattering Spectrometry (RBS) which is a thin film analysis technique

Read More »
IGA

IGA Webinar

This webinar will focus on Instrumental Gas Analysis (IGA) that measures gas-forming elements present in solid materials.

Read More »

To enable certain features and improve your experience with us, this site stores cookies on your computer. Please click Continue to provide your authorization and permanently remove this message.

To find out more, please see our privacy policy.