Clinical Stage Resources for Life Science Organizations

Veeva R&D Quality Summit 2022 

As a Premiere Services Partner, USDM has been helping Veeva customers reduce their implementation and validation time since 2015, with over 200 Veeva projects successfully completed. Visit our booth at Veeva’s R&D and Quality Summit in Boston.

Darlene Limtiaco
- September 19, 2022

News & Events

Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma

Clinical, Information Technology for Life Science Organizations, Manufacturing, Quality Assurance for Life Science Organizations, Regulatory

Computer Software Assurance (CSA) Draft Guidance Webinar

UPCOMING WEBINAR: Please join our panel of experts, including Francisco Vicenty, Program Manager, Case for Quality, FDA, to discuss any changes and implications impacting medical devices, pharma, and biotech organizations.

Webinars

Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma

Clinical, Information Technology for Life Science Organizations, Quality Assurance for Life Science Organizations, Regulatory

Meet with us at Bio International 2022 in San Diego

Our Emerging Leadership Team will be attending #BIO2022 and we invite you to meet with them to discuss how we help startups establish their overall IT strategy and rapidly execute a compliant IT framework.

Lisa Om
- June 1, 2022

News & Events

Biotech

Clinical, Information Technology for Life Science Organizations, Regulatory

Automating Validation Across Your Tech Stack

ON-DEMAND WEBINAR: This webinar will addresses forward-thinking validation and continuous compliance considerations for modern cloud technologies.

Webinars

Biotech, Medical Device, Pharma

Clinical, Information Technology for Life Science Organizations, Quality Assurance for Life Science Organizations, Regulatory

Process Automation for Regulated GxP Workflows

ON-DEMAND WEBINAR: Learn how USDM customized various workflows, demonstrated a framework for continuous compliance, and responded to detailed questions about regulatory requirements for each of the featured customers.

Webinars

Biotech, Medical Device, Pharma

Clinical

Box Meets Complex Security and Global GxP Validation Requirements

Case study on Box Meets Complex Security and Global GxP Validation Requirements.

David Blewitt
- April 24, 2022

Case Studies

Biotech

Clinical, Regulatory