Reimagining Medical Device Post-Market Surveillance On-demand webinar topic: Reimagining Medical Device Post-Market Surveillance. Webinars Medical Device Manufacturing, Quality Assurance
Q&A: SaMD Regulations and Compliant Development Environments Blog article written from the Q&A during the SaMD Regulations and Compliant Development Environments webinar. Various Authors - February 13, 2022 Blogs Medical Device Information Technology, Regulatory
Complaint Handling Integration with Salesforce Improves Patient Care Case study on Complaint Handling Integration with Salesforce Improves Patient Care. Jim Macdonell - February 12, 2022 Case Studies Medical Device Information Technology, Regulatory
The Origins of UDI Blog article topic: The Origins of UDI. Jay Crowley - February 11, 2022 Blogs Medical Device Manufacturing, Regulatory, Safety
GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Blog article topic: GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Diane Gleinser - February 10, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
Your IT Roadmap – Guidance for Early-Stage Life Sciences Startups Learn how to create a strategic IT roadmap for early-stage life sciences companies. Address functional needs, GxP compliance, and adapt to evolving demands. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Research & Development
