Seminare zu Pharma / Medical devices
Pharma / Medical devices
High-quality courses and training for
pharma and healthcare professionals

Results FOR "Pharma / Medical devices"

SORT RESULTS

High-quality training in regulatory affairs and pharmacovigilance

Our regulatory courses and conferences are presented by established experts who will provide you with practical information on the fundamentals and trends in marketing authorisation, regulatory maintenance and post-marketing surveillance.

  • More Information / Overview

PharmaFORUM Webcast International "eCTD worldwide"

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
  • Online / 01.11. - 31.10.2020

PharmaFORUM Webcast Biologics "Interaction with Agencies"

Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.

  • Online /
  • Online / 01. - 31.01.2020
  • Online / 01. - 29.02.2020
  • Online / 01. - 31.03.2020
  • Online / 01. - 30.04.2020
  • Online / 01. - 31.05.2020
  • Online / 01. - 30.06.2020
  • Online / 01. - 31.07.2020
  • Online / 01. - 31.08.2020
  • Online / 01. - 30.09.2020
  • Online / 01. - 31.10.2020

PharmaFORUM Webcast Biologics "QbD elements in early and late stage biotherapeutic development (from research to first in human until commercial)"

Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.

  • Online /
  • Online / 01. - 31.01.2020
  • Online / 01. - 29.02.2020
  • Online / 01. - 31.03.2020
  • Online / 01. - 30.04.2020
  • Online / 01. - 31.05.2020
  • Online / 01. - 30.06.2020
  • Online / 01. - 31.07.2020
  • Online / 01. - 31.08.2020
  • Online / 01. - 30.09.2020
  • Online / 01. - 31.10.2020

PharmaFORUM Webcast International "Pharmaceutical Documentation and CMC Strategy"

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
  • Online / 01.11. - 31.10.2020

PharmaFORUM Webcast Biologics "Quality of Biotech-IMPs - the current challenges"

Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.

  • Online /
  • Online / 01. - 31.01.2020
  • Online / 01. - 29.02.2020
  • Online / 01. - 31.03.2020
  • Online / 01. - 30.04.2020
  • Online / 01. - 31.05.2020
  • Online / 01. - 30.06.2020
  • Online / 01. - 31.07.2020
  • Online / 01. - 31.08.2020
  • Online / 01. - 30.09.2020
  • Online / 01. - 31.10.2020

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 / 31.12.2019

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 / 31.12.2019

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 / 31.12.2019

e-Learning: Stability Testing in the ICH Region

This e-Learning programme will focus on stability testing for chemical and biological products in the ICH region.

  • Online /
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