Accelerating Compliance for Better Business Outcomes Case study on Accelerating Compliance for Better Business Outcomes. Erin Christy - February 5, 2022 Case Studies Medical Device Information Technology, Regulatory
FAQ: CSV, CSA, and Why the Paradigm Shift This FAQ curates many questions from our customers and attendees to our various webinars with the FDA on the CSA Guidance. Sandy Hedberg - February 2, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
An Introduction to Computer System Validation On-demand webinar topic: An Introduction to Computer System Validation. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Cloud Content Management with Automated GxP Compliance Built In Download this white paper and learn how you can securely share data with partners, vendors, and regulators while complying with GxP requirements globally. Various Authors - January 15, 2022 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Quality Assurance
Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? Blog article topic: Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? Diane Gleinser - January 13, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
Benefits of Pharmaceutical Serialization Blog article topic: Benefits of Pharmaceutical Serialization. Jim Macdonell - January 9, 2022 Blogs Pharma Regulatory, Safety
