Clinical Research
Regulatory expertise and practical insights for your work in clinical trials. From early Phase I through to non-interventional studies – comprehensive knowledge covering all areas.
Thema
Dates
Format
Early Phase Complex Clinical Trials
Do you want to strategically plan your early phase clinical trials (phase I/IIa) from the start to accelerate drug development? Then get tips and hands-on experience regarding traditional and complex…Language: English
25/09/2026
Online-Seminar
Details
e-Learning: Good Clinical Practice - GCP in the EU and Germany
The fundamentals of Good Clinical Practice - use this e-learning course to build a solid basis for your work in clinical drug trials in the EU and in Germany. Learn what it means to plan and conduct…Language: English
available immediately
e-Learning
Details
EU Biotech Act: What Pharma R&D Professionals need to know
The EU Biotech Act is still evolving - but preparation cannot wait. Join experts from authority and industry to understand what is coming, what remains uncertain, and how to get your R&D…Language: English
17/11/2026
Online-Seminar
Details
CTD: requirements for non-clinical/clinical modules and eCTD-readiness
Non-clinical/clinical content in the dossier: Are you a beginner in the field and would like to feel confident working competently on modules 2, 4 and 5 in the future? Are you already an experienced…Language: English
21 - 22/09/2026
Online-Seminar
Details
Contact
We are happy to provide you with personal and individual advice.
Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.
Regine Görner, Dr. Verena Klüver
r.goerner@forum-institut.de
v.kluever@forum-institut.de