The Direct Marking of Medical Devices in the U.S. and Europe White paper on The Direct Marking of Medical Devices in the U.S. and Europe. Jay Crowley - April 18, 2021 White Papers Medical Device Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Caution about FDA’s Most Recent UDI “Enforcement Discretion” Guidance Blog article topic: Caution about FDA’s Most Recent UDI “Enforcement Discretion” Guidance. Jay Crowley - April 13, 2021 Blogs Medical Device Manufacturing, Regulatory
Computer Software Assurance: What You Need to Know About the FDA’s Upcoming Guidance White paper on Computer Software Assurance: What You Need to Know About the FDA’s Upcoming Guidance. Sandy Hedberg - January 15, 2021 White Papers Biotech, CMO, CRO, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
More Medical Device Implications of Brexit Blog article topic: More Medical Device Implications of Brexit. Jay Crowley - January 12, 2021 Blogs Medical Device Manufacturing, Regulatory
2021 Life Sciences Trends White paper on 2021 Life Sciences Trends. Various Authors - November 6, 2020 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Using PTC’s ThingWorx Solution in a GxP Regulated Environment White paper on Using PTC’s ThingWorx Solution in a GxP Regulated Environment. Concha Luque - July 26, 2020 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance
