IDMP: How Did We Get Here, and What Does That Mean for Me?Mladen Prenc2024-09-16T18:01:43+00:00July 7, 2022|Read More
How Clinical Operations Can Accelerate Through De-risking Clinical TrialsMladen Prenc2022-06-13T16:22:45+00:00June 13, 2022|Read More
How to Ensure a Full-Proof IDMP Strategy in 3 StepsMladen Prenc2022-06-08T15:52:45+00:00June 8, 2022|Read More
Staying Ahead of ICH E6(R3) Good Clinical Practice GuidelinesMladen Prenc2022-05-17T16:33:42+00:00May 17, 2022|Read More
COVID-19 and Vaccine Safety Brings Pharmacovigilance Center StageMladen Prenc2022-05-13T16:38:36+00:00May 13, 2022|Read More
The Risks and Rewards of Decentralized Clinical TrialsMladen Prenc2022-05-12T16:50:23+00:00May 12, 2022|Read More
How RIMS Help Manage Increasing Complexity in Regulatory AffairsMladen Prenc2022-04-18T09:00:31+00:00April 18, 2022|Read More
Benefits of Integrating Your Medical Information and Safety WorkflowsMladen Prenc2022-03-30T09:00:03+00:00March 30, 2022|Read More
Synergy and Efficiencies Within: The Benefits of a Connected Clinical PlatformMladen Prenc2022-03-20T09:00:03+00:00March 20, 2022|Read More
To Prepare for IDMP, Organizations Must Think Years Ahead – Not MonthsMladen Prenc2022-03-07T09:00:36+00:00March 7, 2022|Read More
Key Features of eTMF Systems for Clinical Trial SuccessMladen Prenc2022-02-28T09:15:13+00:00February 28, 2022|Read More
Checklist: Essential Features of a Future-Proof Automated eTMF SystemMladen Prenc2022-02-22T15:35:57+00:00February 22, 2022|Read More