"This is the best use of my time to remain current with what is going on in the industry."
Submission of comments on EMA’s draft “Guideline on computerised systems and electronic data in clinical trials”
These comments are provided by a team with representatives from 13 eCF member companies and have been reviewed by the eClinical Forum members. Those on the team are from Sweden, UK, Switzerland, Belgium, Spain, Germany, Italy, United States, and Japan. They represent many hours of personal review/comment as well as 19 hours of team discussion. The larger eCF Membership had opportunity to review and comment as well. The resulting submitted comments (59 pages) are a consensus of member opinion.
Webinar "AI Validation"
As generative and agentic AI become part of pharmaceutical operations, how do we validate these systems in a practical way? If you are interested in this topic, join our webinar on June 24th 2026!