Medical device manufacturers around the world are working to ensure their package designs are in line with the recent updates to ISO 11607, Part 1 and Part 2, and the Medical Device Regulation...
WuXi AppTec Welcomes Sherry Parker, Ph.D., as Senior Director of Regulatory Toxicology
Regulatory, validation, Reprocessing, MDR, Class Ir, Reusable Device
Today’s regulatory environment requires top-notch partners to help navigate preclinical testing. With that in mind, WuXi AppTec is very excited to announce the return of Dr. Sherry Parker! Dr....
Preparing for MDR: Don’t Forget about Class I Reusable Devices
Regulatory, validation, Reprocessing, MDR, Class Ir, Reusable Device
Medical device manufacturers are busy preparing for the about MDR and Class III device changes. As you work through your portfolio and sort your products into families, you’ll face many tough...
Q1 Productions 8th Annual Packaging Conference
Medical Device, package testing, package design, validation
WuXi AppTec is proud to be a sponsor at Q1 Productions’ 8th Annual Medical Device Packaging Conference, May 15-16, 2018, in Chicago, Illinois.