Top 10 Considerations for Implementing a GxP Content Management System Discover the top 10 considerations for implementing a GxP-compliant content management system to enhance compliance, efficiency, and data management. Hovsep Kirikian - April 5, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
USDM Life Sciences at Validation University By KENX, Validation University is a 3 day conference that shares knowledge & best practices for validation in life sciences. Ryan McDonald - March 18, 2024 News & Events Biotech, Medical Device, Pharma Information Technology
Good Machine Learning Practice (GMLP) for Medical Device Development: Guiding Principals Explore the guiding principles of Good Machine Learning Practice (GMLP) and the importance of ethics, data integrity, and model transparency. Jim Macdonell - March 15, 2024 Blogs Medical Device Information Technology, Regulatory
2024 Trends in Life Sciences Life sciences organizations are eager to make use of their vast amounts of data. Explore five trends that are fueling their efforts. Various Authors - March 8, 2024 White Papers Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance
A Few Surprises in FDA’s Quality Management System Regulation For most manufacturers, the new QMSR will simplify their approach to quality system compliance. Learn about two important issues to be aware of. Jay Crowley - March 1, 2024 Blogs Medical Device Regulatory
Lessons Learned in the On-Going RPA Journey Blog article topic: Lessons Learned in the On-Going RPA Journey. Ryan McDonald - February 22, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
