Webcode 10019
01/01/-31/12/2025
01/01/-31/12/2025
online
online
Veranstaltung - 4,500 € zzgl. MwSt.
The fee includes course documentation for download and a certificate.
Veranstaltung - 4,500 € zzgl. MwSt.
The fee includes course documentation for download and a certificate.
Dr. Birgit Wessels
Conference Manager
+49 6221 500-652
b.wessels@forum-institut.de
With this qualification course, you can continue your education in a structured manner in all CMC topics, with a technical focus on development methods, manufacturing processes, CMC documents, change management, and much more.
Would you like to have profound know-how in CMC topics, remain flexible in terms of time and set your own content priorities? Then this is right for you.
The concept: You start with a two-day basic seminar "CMC Management in Regulatory Affairs" (talking about the english course) and then select three further seminar modules (= 3 seminar days) that support your professional development.
You will qualify as a CMC-Specialist in a maximum of 18 months (or in just a few weeks) and receive certification from the FORUM Institute.
In this way, you can achieve your training goal efficiently and precisely.
This qualification course is aimed at employees of the pharmaceutical industry and their service providers who require in-depth know-how in CMC topics.
You attend the two-day basic course "CMC Management in Regulatory Affairs".
Afterwards you participate in 3 further modules (= seminar days), possible options we have mentioned here.
Alternative seminar modules from our portfolio can be selected and we are even happy to design new seminars on request. Please contact us!
CMC requirements in Latin America with focus Mexico, Brazil, Colombia, Argentina, Chile, and Peru. The seminar (2 half d...
Experts from national competent authorities speak about the current developments with regard to e.g. the revision of gui...
Get your know-how on creating and maintaining quality data for biotech products in our online training.
CMC dossier requirements FDA vs EU: After having attended the seminar you will feel secure writing and maintaining the q...
You as "beginner" or "refresher" would like to feel more secure writing CMC documents? Our experts will provide you with...
Das Online-Seminar zu den Themen Entwicklung, Qualität, CMC, Zulassung und Market Access für ATMPs.
Are you a specialist in the pharmaceutical industry in the area of marketing authorization and responsible for compiling...
Four live webcasts à 2 hours every week: CMC requirements in China, India, Japan, South Korea and Russia/EAEU. Meet our ...
Global regulatory requirements for drug device combination products (DDCs): You will receive a regulatory overview for t...
This e-Learning programme will familiarise you with the data requirements in CTD Module 3.
Details
This online training will give you in-depth knowledge on the CMC requirements for marketing authorisation. Take the chan...
Details
This online training will give you in-depth knowledge on the CMC requirements for marketing authorisation. Take the chan...
Details
