Seminare zu Online-Training
Online-Training
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Global Regulatory Affairs Manager

This online training addresses the needs of regulatory affairs managers dealing with marketing authorisations outside the EU or planning to do so in the future.

  • Modular e-Learning and webcast / Access possible at any time

Development Expert Biologics

  • Modular e-Learning and webcast / Access possible at any time

PharmaFORUM Webcast Biologics

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 /

PharmaFORUM Webcast International

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 /

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 /

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 /

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 /

Webcast Series: Legal Issues in Regulatory Affairs

These six webcasts enable you to deal with the legal challenges in marketing authorisation and life cycle management.

  • Online /

eCTD preparation and submission

This online training programme consisting of three recorded webcasts will train you how to develop documents, compile them and submit an eCTD step by step.

  • Online /

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 /

e-Learning: CTD Module 3

This e-Learning programme will familiarise you with the data requirements in CTD Module 3.

  • Online /

Pharmacovigilance in Europe - Introductory webcast series

Do you need to be well versed in European pharmacovigilance for your daily work? Then we would like to invite you to join this webcast series. You can choose between three different packages according to your level of expertise and requirements.

  • Online /

First Accredited Diploma in Pharmacovigilance for the Middle East

First Accredited Diploma in Pharmacovigilance for the Middle East

  • Online /

Educational material in Europe

Educational material will remain a national issue in each European country. Familiarise yourself with the regulations in the Netherlands, France, Switzerland, Italy and Germany in this webcast series consisting of six webcasts.

  • Online /
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