GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Blog article topic: GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Diane Gleinser - February 10, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
5 Tips to Drive Your IT and Compliance Strategy for IT Leaders in Emerging Life Sciences Blog article topic: 5 Tips to Drive Your IT and Compliance Strategy for IT Leaders in Emerging Life Sciences. Erin Christy - February 8, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Your Compliance and Technology Today Watch replays from USDM’s Forward-Thinking GxP Compliance & Process Optimization event. Learn about compliance maturity, IT roadmaps, and process harmonization. Roger Davy - January 28, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Auditing-as-a-Service Delivered 80% More Efficient Audits Case Study: USDM revamps antiquated auditing process to save customer’s time and money Bob Lucchesi - January 18, 2022 Case Studies Biotech Quality Assurance, Safety
The Cannabis Industry: Compliance and Enforcement in an Ever-Changing Regulatory Environment Blog article topic: The Cannabis Industry: Compliance and Enforcement in an Ever-Changing Regulatory Environment. Joseph Cassella - January 8, 2022 Blogs Pharma Quality Assurance, Regulatory
2022 Trends in Life Sciences White paper on 2022 Trends in Life Sciences. Various Authors - November 4, 2021 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
