Q&A: EU MDR Date of Application Readiness Blog article written from the Q&A during the EU MDR Date of Application Readiness webinar. Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Optimized Use of TraceLink Helps Pharma Company Implement Serialization Case study on Optimized Use of TraceLink Helps Pharma Company Implement Serialization. Erin Christy - April 18, 2022 Case Studies Pharma Information Technology, Regulatory
Box GxP for Controlled Clinical Management Case study on Box GxP for Controlled Clinical Management. Kim Hutchings - April 18, 2022 Case Studies Pharma Clinical, Information Technology, Research & Development
Is There a Checklist for GCP Audits? Blog article topic: Is There a Checklist for GCP Audits? Bob Lucchesi - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
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. 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. Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
