Webcode 22122046
with several local experts
EU and non-EU regulatory affairs experts share their knowledge with you
anytime
anytime
online
online
Event - 3.900,- € plus tax
The fee includes the access to the PharmaFORUM Webcast international library, six two hour webcasts and a choice of four live seminar days (including course documentation and certificate).
Event - 3.900,- € plus tax
The fee includes the access to the PharmaFORUM Webcast international library, six two hour webcasts and a choice of four live seminar days (including course documentation and certificate).
Dr. Henriette Wolf-Klein
Head of Department
+49 6221 500-680
h.wolf-klein@forum-institut.de
This qualifying course is tailoured to your needs - you choose the regulatory information you need and attend the courses you like to.
Do you work in global regulatory affairs, dealing with EU and non-EU issues?
Do you need an update on single markets outside the familiar European regulatory framework?
Then, this 'Global Regulatory Affairs Manager' qualifying course will be just what you need.
The training programme includes:
1.) A year's membership of the PharmaFORUM Webcast International series with access to more than 25 videos and related training material
2.) Six live two-hour webcasts from the PharmaFORUM Webcast International series on India, Iran, Iraq, China and more
3.) Your choice of four days of live online seminars within 18 months
This qualifying course is intended for anyone working in global regulatory affairs needing strategic know-how and practical insights into specific markets all over the world.
A year's membership of the PharmaFORUM Webcast International with access to more than 25 videos and related training material is granted to you. This also includes six live two-hour webcasts on India, Iran, Iraq, China and more in 2022
You can choose four days of live online seminars within 18 months. You can choose these seminars from this website This includes seminars as
Regulatory Affairs in the US (1 day spread over 2 half days)
Regulatory Affairs in China and the ASEAN CTD (2 days)
Regulatory Affairs and CMC in Russia (2 days)
Regulatory Affairs in Japan (1 day)
Regulatory Affairs in Latin America (2 days)
and much more
Overall score of all evaluations in 2021
Five stars on Trustpilot = Excellent
The course provides practical, hands-on experience in eCTD specifications, eSubmission requirements and data integrity f...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
Our biotech experts will provide you with the latest information on issues related to development, quality and regulator...
Our biotech experts will provide you with the latest information on issues related to development, quality and regulator...
Here you can find the technical requirements for our online events that must be met.
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Try out our e-Learning programmes free of charge and without any obligation.
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We provide flexible education and training with high-quality e-Learning programmes for several topics.
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