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Reimagining Medical Device Post-Market Surveillance On-demand webinar topic: Reimagining Medical Device Post-Market Surveillance. 0 Webinars Medical Device Manufacturing, Quality Assurance
The Origins of UDI Blog article topic: The Origins of UDI. 0 Jay Crowley - February 11, 2022 Blogs Medical Device Manufacturing, Regulatory, Safety
Complaints Remediation to Meet FDA Consent Decree Deadline Case study on Complaints Remediation to Meet FDA Consent Decree Deadline. Jim Macdonell - February 7, 2022 Case Studies Medical Device Manufacturing
Computer Software Assurance (CSA) Guidance White paper on Computer Software Assurance Guidance. 1 Sandy Hedberg - February 3, 2022 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
Key differences in the requirements for SFDA UDI and US & EU UDI Blog article topic: Key differences in the requirements for SFDA UDI and US & EU UDI. 0 Jay Crowley - January 29, 2022 Blogs Medical Device Manufacturing, Regulatory
