by Tepsivo | Feb 28, 2025 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction Tepsivo’s AI Journey The Idea of Tepsivo AI Test Results of AI in Drug Safety Assessment Our Learnings What’s Next for AI in PV? 2025 is the Year of AI in...
by Tepsivo | Jan 30, 2025 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction What to expect? EMA signal pilot is ending Public feedback for the amendment Amendments with Tepsivo’s commentary Amendment 1 Amendment 2 Amendment 3 Amendment 4...
by Tepsivo | Dec 9, 2024 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction GxP in EU Legislation GVP in EU Legislation GDP and GMP in EU Legislation GCP in EU Legislation Referring to Legal Requirements in GVP Recommendations and Requirements in GxP...
by Tepsivo | Oct 25, 2024 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction A Public Beta Getting Started Portal Access Navigating the Portal Application Statuses Video Demonstration Portal Features Conclusion What is MHRA’s RegulatoryConnect Portal?...
by Tepsivo | Oct 17, 2024 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction A flea market Lectures Point of going Giving a speech Obvious bias A final note Pharmacovigilance conferences are a flea market Written by Dominik Hodbod | Oct 17, 2024 This...
by Tepsivo | May 22, 2024 | Blog
No time to read now? -> Download the article as a handy pdf List of contents Introduction Part 1: EMA Website Part 2: Other parts of the legislation Part 3: Guidelines Part 4: Dialog with EMA Our questions Response from EMA Conclusion Interpreting fuzzy...
Recent Comments