Webcode 10019
01/01/-31/12/2024
01/01/-31/12/2024
online
online
Veranstaltung - 4,000 € zzgl. MwSt.
The fee includes course documentation for download and a certificate.
Veranstaltung - 4,000 € 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!
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Get your know-how on creating and maintaining quality data for biotech products in our online training.
LAST CALL! - REGISTRATION DEADLINE: 02.10.2024 - CMC requirements in the US: After having attended the seminar you will ...
LAST CALL! - REGISTRATION DEADLINE: 15.10.2024 - FDA inspection readiness: Gain the knowledge and skills necessary to ma...
