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
Selecting, Implementing, and Maintaining Cloud Systems for the Life Sciences Industry White paper on Selecting, Implementing, and Maintaining Cloud Systems for the Life Sciences Industry. David Blewitt - May 24, 2020 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
