Master Data Management and Validation to Meet Global Requirements Case study on Master Data Management and Validation to Meet Global Requirements. Jay Crowley - April 7, 2022 Case Studies Medical Device Information Technology, Quality Assurance, Regulatory
Rapid Application Migration Blog article topic: Rapid Application Migration. Stepheni Norton - April 4, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Top 10 Recurring Audit Observations at Life Sciences Companies Blog article topic: Top 10 Recurring Audit Observations at Life Sciences Companies. Bob Lucchesi - April 3, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
Oracle Validation and Assurance Virtual Roundtable On-demand webinar topic: Oracle Validation and Assurance Virtual Roundtable. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Customized CPET Analysis Workbook Case study on Customized CPET Analysis Workbook. Hovsep Kirikian - April 2, 2022 Case Studies Pharma Clinical, Information Technology, Quality Assurance, Regulatory
Update from the FDA on CSV Changes On-demand webinar topic: Update from the FDA on CSV Changes. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
