Medical Device Testing

Eurofins E&E Is Now An FDA ASCA-Accredited Laboratory For Medical Device Testing

On April 12th, 2021, Eurofins E&E North America, an accredited ISO/IEC 17025 test laboratory, achieved ASCA recognition by the U.S. Food and Drug Administration (FDA), for Premarket Testing of Medical Devices. Launched on September 25th, 2020, the voluntary  Accreditation Scheme for Conformity Assessment (ASCA) Pilot Program was devised to enhance consistency and predictability in the... Read More