Pharmaceutical IT & Regulatory Compliance Resources

GxP Training in Today’s Regulatory and Technology Landscape

Modern GxP training with VR, AI, and blockchain boosts compliance, minimizes risks, and improves ROI, ensuring quality, safety, and efficiency in life sciences.

Lisa Om
- October 21, 2024

Blogs

Biotech, CMO, CRO, Medical Device, Pharma

Quality Assurance, Regulatory

LLMs and Cybersecurity Standards in Life Sciences

LLMs present opportunities to advance drug discovery and development, but protecting the data being processed takes precedence.

Brian Rankin
- October 16, 2024

Blogs

Biotech, Medical Device, Pharma

Clinical, Information Technology, Regulatory

Modernize Your Audits and Compliance with Tech Innovations

Discover how GenAI, AR/VR, and IoT are transforming life sciences audits by improving compliance accuracy, reducing costs, and enabling proactive risk management.

Lisa Om
- October 3, 2024

Blogs

Biotech, CMO, CRO, Medical Device, Pharma

Quality Assurance, Regulatory

USDM Life Sciences at BoxWorks 2024

See the future of intelligent content management and AI-powered products that automate your workflows and secure your data.

Michelle Gardner
- September 27, 2024

News & Events

Biotech, CMO, CRO, Pharma

Information Technology, Regulatory

Good Automated Manufacturing Practice vs. Computer Software Assurance

CSA modernizes and refines GAMP 5 practices to make validation more efficient without compromising system quality or compliance.

Jim Macdonell
- September 23, 2024

Blogs

CMO, Medical Device, Pharma

Manufacturing, Quality Assurance

Achieving Unprecedented Value from your Veeva Investments

Maximize your Veeva investment with USDM. Solve data silos, integration barriers, and platform complexities with tailored, compliance-ready solutions.

Lisa Om
- September 17, 2024

Blogs

Biotech, Medical Device, Pharma

Information Technology