How Do Life Science Companies Qualify Vendors and Software? Automated equipment & systems used by companies are supplied by vendors & are purchased off-the-shelf (OTS). They should audit the vendors development. 0 David Blewitt - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
Five Tips for Successful Veeva Implementation Blog article topic: Five Tips for Successful Veeva Implementation. 0 Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
FDA CBD Enforcement Report Released to Congress Blog article topic: FDA CBD Enforcement Report Released to Congress. 0 Joseph Cassella - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Virtual Audits and Inspections On-demand webinar topic: Virtual Audits and Inspections. 1 Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
How to Get Results on Regulated Projects with Virtual Teams On-demand webinar topic: How to Get Results on Regulated Projects with Virtual Teams 0 Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Research & Development
Cybersecurity Threats and Risks to Life Sciences Companies On-demand webinar topic: Cybersecurity Threats and Risks to Life Sciences Companies. 0 Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology
