EMA & FDA Alignment on ISO IDMP: Transforming the E2B Safety Database LandscapeMladen Prenc2026-01-20T14:28:27+00:00January 20, 2026|Read More
Guiding principles: how new CIOMS XIV guidance will accelerate trusted AI use in regulated contextsMladen Prenc2026-01-29T19:22:32+00:00January 15, 2026|Read More
AI in PV case intake & processing: where are we now?Mladen Prenc2026-01-09T10:24:29+00:00January 9, 2026|Read More
How AI and Automation Improve the Entire PV EcosystemMladen Prenc2025-12-04T15:51:45+00:00December 4, 2025|Read More
How to Make Your Case to Attend Breakthrough 2026Â fcampbell@arisglobal.com2025-11-11T09:04:56+00:00November 3, 2025|Read More
Frost & Sullivan Recognizes ArisGlobal’s MedDRA Coding Agent InnovationMladen Prenc2026-01-07T08:07:36+00:00October 23, 2025|Read More
Operationalizing AI Across the End-to-End Safety Ecosystem Mladen Prenc2025-11-05T11:29:21+00:00October 15, 2025|Read More
5 Reasons You Can’t Miss Breakthrough 2026Mladen Prenc2025-10-21T15:31:49+00:00September 22, 2025|Read More
Driving Digital Transformation in Pharma: Why Change Management Is Mission-CriticalMladen Prenc2025-08-21T12:58:03+00:00August 21, 2025|Read More
Breakthrough 2026: Madrid | February 10-11Mladen Prenc2025-08-04T15:18:01+00:00August 4, 2025|Read More
Industry Panel Webinar: How GenAI is Changing Regulatory AffairsMladen Prenc2025-08-04T15:18:54+00:00August 4, 2025|Read More
Navigate the FDA’s E2B(R3) Mandate with Confidence – Powered by LifeSphere MultiVigilanceMladen Prenc2025-07-30T22:31:29+00:00July 30, 2025|Read More
