Validating SharePoint for Life Sciences Regulated Environments Blog article topic: Qualifying SharePoint for Life Sciences Regulated Environments. 0 Hovsep Kirikian - April 11, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Single Sign-on Significantly Improves Security and Usability Blog article topic: Single Sign-on Significantly Improves Security and Usability. 0 Lisa Om - April 7, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
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
Improved UDI Data Integrity with Single-Source-of-Truth Case study on Improved UDI Data Integrity with Single-Source-of-Truth. Jay Crowley - April 5, 2022 Case Studies Medical Device Manufacturing
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
MDSAP Ready in 4 Months Through Assessment and Remediation Case study on MDSAP Ready in 4 Months Through Assessment and Remediation. Jim Macdonell - April 1, 2022 Case Studies Medical Device Clinical, Manufacturing, Regulatory
