Reimagining Medical Device Post-Market Surveillance On-demand webinar topic: Reimagining Medical Device Post-Market Surveillance. 0 Webinars Medical Device Manufacturing, Quality Assurance
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? 0 Diane Gleinser - February 10, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
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
Auditing-as-a-Service Delivered 80% More Efficient Audits Case Study: USDM revamps antiquated auditing process to save customer’s time and money 0 Bob Lucchesi - January 18, 2022 Case Studies Biotech Quality Assurance, Safety
EU MDR Date of Application Readiness Guide White paper on EU MDR Date of Application Readiness Guide. 0 Jay Crowley - January 17, 2022 White Papers Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
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. 0 Various Authors - January 15, 2022 White Papers Biotech, Medical Device, Pharma Clinical, Information Technology, Quality Assurance
