Streamlining Clinical Trials with the LLM Protocol Assistant LLM Protocol Assistant improved clinical trial efficiency, reducing costs by $250K annually, cutting protocol queries by 70%, and accelerating timelines by 15%. Darlene Limtiaco - December 2, 2024 Case Studies Biotech, Pharma Clinical, Information Technology, Regulatory
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
Drive Business Growth and Efficiency with a Strategic Data Roadmap A strategic data roadmap fosters growth, compliance, and innovation in life sciences by centralizing, optimizing, and scaling data management systems. Lisa Om - November 23, 2024 Blogs Biotech, Pharma Clinical, Information Technology, Regulatory
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
Oracle CloudWorld 2024 – Life Sciences Lunch & Learn If you’re attending Oracle CloudWorld, then you’re invited to an exclusive Life Sciences Lunch & Learn. Register today! Michelle Gardner - July 24, 2024 News & Events Biotech, Medical Device, Pharma Information Technology, Regulatory
Manual Testing vs. Automated Testing Explore the key differences between manual and automated testing and discover the benefits of automated regression testing. Hovsep Kirikian - July 17, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
