Regulated GxP Workloads in the Public Cloud White paper on Regulated GxP Workloads in the Public Cloud. 0 John Petrakis - May 17, 2021 White Papers Biotech, Medical Device, Pharma Clinical, Manufacturing, Research & Development
Best Practices for Virtual Audits and Regulatory Inspections White paper on Best Practices for Virtual Audits and Regulatory Inspections. 0 Bob Lucchesi - February 18, 2021 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
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. 0 Sandy Hedberg - January 15, 2021 White Papers Biotech, CMO, CRO, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
2021 Life Sciences Trends White paper on 2021 Life Sciences Trends. 0 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. 0 Concha Luque - July 26, 2020 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance
Quality Management Systems for Emerging Life Sciences Organizations 0 Roger Davy - July 16, 2020 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Regulatory
