Seminare zu Regulatory affairs & vigilance
Regulatory affairs & vigilance
Regulatory training programmes and courses
you should not miss.

Results FOR "Regulatory affairs & vigilance"

SORT RESULTS

PharmaFORUM Webcast International "Marketing authorisation in Turkey"

Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!

  • Online /
  • Online / 01.01. - 31.12.2019
  • Online / 01.03. - 29.02.2020
  • Online / 01.05. - 30.04.2020
  • Online / 01.07. - 30.06.2020
  • Online / 01.09. - 31.08.2020

e-Learning: Introduction to EU Marketing Authorisation

This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).

  • Online /
  • Online / 31.12.2018

e-Learning: Marketing Authorisation Outside the ICH Region

This e-learning will familiarise you with the regulatory affairs principles outside the ICH region and show you how to categorise the various regions in terms of regulatory requirements. Dossier requirements in Australia, Hong Kong, India, South Korea, Taiwan, Saudi Arabia, GCC, Jordan, Turkey, Thailand, China, South Africa, Russia, Kazakhstan, Eqypt, Brazil, Mexico & Argentina will be addressed

  • Online /
  • Online / 31.12.2018

e-Learning: Common Technical Document & eCTD

Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeable in this field. No prior dossier experience is required.

  • Online /
  • Online / 31.12.2018

First Accredited Diploma in Pharmacovigilance for the Middle East

First Accredited Diploma in Pharmacovigilance for the Middle East

  • Online /
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