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
Quality System Upgrade to Meet EU MDR and EU IVDR Case study on Quality System Upgrade to Meet EU MDR and EU IVDR. Jay Crowley - March 18, 2022 Case Studies Medical Device Manufacturing, Regulatory
Accelerating Cloud Content Management for Emerging Life Sciences On-demand webinar topic: Accelerating Cloud Content Management for Emerging Life Sciences. 0 Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology
GxP QMS Framework Prepares Emerging Biopharma for Commercialization Case study on GxP QMS Framework Prepares Emerging Biopharma for Commercialization. Erin Christy - March 3, 2022 Case Studies Biotech, Pharma Clinical
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
Onsite and Remote On-Demand Compliance Staff Augmentation Case study on Onsite and Remote On-Demand Compliance Staff Augmentation. Vega Finucan - February 6, 2022 Case Studies CMO, CRO Information Technology, Regulatory
