Best Practices for Managing Content in Emerging Biopharma and Regulated Life Sciences Companies Streamline content management for emerging biopharma with best practices to ensure compliance, scalability, and operational excellence Lisa Om - November 25, 2024 Blogs Biotech, Pharma Clinical, Information Technology, Research & Development
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
USDM’s Guide to 21 CFR Part 11 Learn about 21 CFR Part 11, the FDA regulation ensuring the security, traceability, and compliance of electronic records and eSignatures in life sciences. David Blewitt - April 14, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Fast-Track Your Journey to Commercialization Fast-track commercialization in life sciences with USDM's GxP expertise, IT strategies, and QMS frameworks for compliance, efficiency, and success. Lisa Om - March 25, 2024 Blogs Biotech Clinical
USDM Life Sciences at the Bio-IT Conference & Expo Meet with USDM Life Sciences at the Box Booth at Bio-It Conference & Expo Ryan McDonald - March 8, 2024 News & Events Biotech Information Technology
GxP System Validation and Monitoring for Half the Cost Learn how an emerging therapeutics company saves more than $400k annually and maintains SaaS systems for half that cost. Lisa Om - June 6, 2023 Case Studies Biotech Information Technology
