Quality Management Archives

Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies

Blog article topic: Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies.

Erin Christy
- March 12, 2022

Blogs

Biotech, CMO, CRO, Medical Device, Pharma

Quality Assurance, Safety

Cellular Therapy Regulations

Blog article topic: Cellular Therapy Regulations.

Diane Gleinser
- March 12, 2022

Blogs

Biotech

Clinical, Regulatory, Research & Development

Q&A with the FDA on CSV Changes

On-demand webinar topic: Q&A with the FDA on CSV Changes.

Webinars

Biotech, CMO, CRO, Medical Device, Pharma

Information Technology, Quality Assurance, Regulatory

Huge Productivity Gains and Decreased Costs with Salesforce

Discover how USDM helped a Fortune 500 medical device manufacturer streamline workflows, save $750K annually, and achieve compliance with Salesforce GxP.

Jim Macdonell
- March 6, 2022

Case Studies

Medical Device

Information Technology, Regulatory

Remanufacturing of Medical Devices, New DIs, and Software Updates

Blog article topic: Remanufacturing of Medical Devices, New DIs, and Software Updates.

Jay Crowley
- March 1, 2022

Blogs

Medical Device

Manufacturing

Top 5 Opportunities to Improve Compliance Maturity

Understand compliance maturity and explore strategies for improvement. Learn how automation, cloud tech, and data-driven approaches drive innovation and compliance.

Various Authors
- February 23, 2022

White Papers

Biotech, CMO, CRO, Medical Device, Pharma

Clinical, Information Technology, Manufacturing, Quality Assurance, Research & Development