Will Your Company Be Ready for the Next Regulatory UDI Database? Blog article topic: Will Your Company Be Ready for the Next Regulatory UDI Database? Jay Crowley - January 14, 2022 Blogs Medical Device Manufacturing, Regulatory
Minimize Risk and Maintain Compliance on Veeva with USDM Cloud Assurance On-demand webinar topic: Minimize Risk and Maintain Compliance on Veeva with USDM Cloud Assurance. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Simplifying Regulated, GxP Business Processes in ServiceNow On-demand webinar topic: Simplifying regulated, GxP business processes in ServiceNow. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
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
The Cannabis Industry: Compliance and Enforcement in an Ever-Changing Regulatory Environment Blog article topic: The Cannabis Industry: Compliance and Enforcement in an Ever-Changing Regulatory Environment. Joseph Cassella - January 8, 2022 Blogs Pharma Quality Assurance, Regulatory
