Maximize eSignature Security with AI in Life Sciences Implementing AI makes it easier than ever to detect fraudulent activities and prevent unauthorized access or post-signing data manipulation in the eSignature approval process. 0 John Petrakis - January 17, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance
Best Practices for Complaint and Adverse Event System Implementation Guidance for data management and system implementation for complaints handling 0 Jim Macdonell - January 3, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
Outsource Your Complaint and Adverse Event Management Blog article topic: Learn the best practices to help get your complaint and adverse event program in place. 0 Jim Macdonell - January 3, 2024 Blogs Medical Device Regulatory
Overcome Workforce Challenges with Augmented Reality Address skills gaps, enhance the training experience, and improve job satisfaction with forward-thinking solutions. 0 Michelle Gardner - December 21, 2023 Blogs Biotech, CMO, Medical Device, Pharma Manufacturing
Anticipating the Use of Generative AI in Life Sciences Global regulatory agencies are not ready for artificial intelligence (AI) that doesn’t have a human in the loop. 0 Michelle Gardner - December 21, 2023 Blogs Biotech, Medical Device, Pharma Information Technology
Cloud Assurance Automation and the Dx Automating workflows and testing for your regulated GxP systems has the potential to save your organization significant time and money. 0 Ryan McDonald - November 1, 2023 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
