Q&A with the FDA on CSV Changes On-demand webinar topic: Q&A with the FDA on CSV Changes. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
Comprehensive SAP Validation Effort, Time Reduced by Over 50% Case study on Comprehensive SAP Validation Effort, Time Reduced by Over 50%. Jim Macdonell - March 7, 2022 Case Studies Pharma Information Technology, Manufacturing, Regulatory
Q&A: Simplifying Regulated GxP Business Processes in ServiceNow Blog article topic: Q&A: Simplifying Regulated GxP Business Processes in ServiceNow. Vega Finucan - March 4, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Biopharma Company Saves $500k by Qualifying Salesforce Case study on Biopharma Company Saves $500k by Qualifying Salesforce. Kim Hutchings - March 1, 2022 Case Studies Biotech, Pharma Information Technology, Regulatory
Top 5 Opportunities to Improve Compliance Maturity Understand compliance maturity and explore strategies for improvement. Learn how automation, cloud tech, and data-driven approaches drive innovation and compliance. Various Authors - February 23, 2022 White Papers Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Research & Development
Computer Software Assurance (CSA) Guidance Explore the FDA's CSA guidance for risk-based computer software assurance in life sciences. Enhance compliance, product quality, and patient safety. Sandy Hedberg - February 3, 2022 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
