2022-06-29 2022-06-29 , online online, 3.900,- € plus tax with several local experts https://www.forum-institut.com/seminar/22122046-qualifying-course-global-regulatory-affairs-manager/referenten/22/22_12/22122046-qualifying-course-global-regulatory-affairs-manager_.jpg Qualifying Course: Global Regulatory Affairs Manager

This qualifying course is tailoured to your needs - you choose the regulatory information you need and attend the courses you like to.

Topics
  • Regulatory affairs EU and non-EU
  • Country specific knowledge (USA, China, Japan, Russia....)
  • Firsthand information from local experts
Aims and objectives
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
Who should attend

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.

22122046 Seminar Qualifying Course: Global Regulatory Affairs Manager

Qualifying Course: Global Regulatory Affairs Manager

Benefits
  • Six two hour webcasts on non-EU regulatory topics
  • Access to an extensive video library
  • Four full-day online seminars to be chosen by you
  • We follow the IMI quality criteria for trainings

Webcode 22122046

Book now

JETZT Buchen

Speaker


Everything at a glance

Appointment

anytime

anytime

Period

Venue

online

online

Fee
Your contact person

Dr. Henriette Wolf-Klein
Head of Department

+49 6221 500-680
h.wolf-klein@forum-institut.de

Details

This qualifying course is tailoured to your needs - you choose the regulatory information you need and attend the courses you like to.

Topics
  • Regulatory affairs EU and non-EU
  • Country specific knowledge (USA, China, Japan, Russia....)
  • Firsthand information from local experts
Aims and objectives

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

Who should attend

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.

Program

A year's membership of the PharmaFORUM Webcast International series
  • This includes access to more than 25 videos and related training material

Six live two-hour webcasts from the PharmaFORUM Webcast International series
  • Regulatory affairs details on India, Iran, Iraq, China and more in live webcast sessions with local experts

Your choice of four days of live online seminars within 18 months
  • Choose four seminar days from our international regulatory affairs training portfolio (4 single days or 2 2-day seminars...)

Trainings details

1. PharmaFORUM Webcast International series

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

2. Your choice of four days of live online seminars

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

Further information

Your Benefits

  • Tailor the training to your needs
  • First-hand information from local regulatory affairs experts
  • Access to a large video library for additional information
  • Share your knowledge with the regulatory affairs community of the PharmaFORUM Webcast International series

You would like to try this offer?

You are interested to attend the Qualifying Course: Global Regulatory Affairs Manager and would like to try it at first free of charge and without any obligation? Please contact me via h.wolf-klein@forum-institut.de or Tel. +49 6221 500 680 and I am happy to offer you a one-week insight into the PharmaFORUM Webcast international series.

This distinguishes our events

Overall score of all evaluations in 2021

Five stars on Trustpilot = Excellent

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