2026-01-23 2026-01-23 , online online, 490 € zzgl. MwSt. e-Learning: CTD Module 3

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

Themen
  • CTD structure and applicable guidelines
  • Drug substance Part
  • ASMF and CEP
  • Drug product part


Who should attend
This e-Learning program addresses the needs of those working in the pharmaceutical industry. It will particularly benefit those needing a good knowledge of the structure and content of CTD Module 3.
Ziel der Veranstaltung
Module 3 is an essential part of the CTD. It presents data on the quality of the drug substance and drug product. But what data is required? How should Module 3 be structured? These are the topics of our e-learning program.
In this e-Learning you will:
  • learn that Module 3 is divided into drug substance and drug product parts
  • take a detailed look at the individual subchapters, their meaning and special requirements
  • get to know what data is essential for the respective subchapters and why
  • and learn the roles of the ASMF and CEP, and how to integrate them into Module 3.
This e-learning was newly created and updated in August 2025.
Teilnehmerkreis

The e-learning format allows you to create your own schedule, pause and rewind the video at any time, and avoid being pressed for time. You will benefit from the long-term experience of the expert Lidia Cánovas and gain a good overview on the important aspects that concern the structure and content of CTD Module 3.

e-Learning: CTD Module 3

e-Learning:
CTD Module 3

- e-Learning -

Benefits
  • Up-to-date expert knowledge
  • Flexibility in location and timing
  • You establish your own learning speed
  • Tests and feedback
  • Officially certified according to ISO 9001 and ISO 21001

Webcode 26122498

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Alles auf einen Blick

Termin

anytime

anytime

Zeitraum

Veranstaltungsort

online

online

Gebühr
Your contact

Dr. Birgit Wessels
Conference Manager

+49 6221 500-652
b.wessels@forum-institut.de

Details

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

Themen

  • CTD structure and applicable guidelines
  • Drug substance Part
  • ASMF and CEP
  • Drug product part


Who should attend
This e-Learning program addresses the needs of those working in the pharmaceutical industry. It will particularly benefit those needing a good knowledge of the structure and content of CTD Module 3.

Ziel der Veranstaltung

Module 3 is an essential part of the CTD. It presents data on the quality of the drug substance and drug product. But what data is required? How should Module 3 be structured? These are the topics of our e-learning program.
In this e-Learning you will:

  • learn that Module 3 is divided into drug substance and drug product parts
  • take a detailed look at the individual subchapters, their meaning and special requirements
  • get to know what data is essential for the respective subchapters and why
  • and learn the roles of the ASMF and CEP, and how to integrate them into Module 3.
This e-learning was newly created and updated in August 2025.

Teilnehmerkreis

The e-learning format allows you to create your own schedule, pause and rewind the video at any time, and avoid being pressed for time. You will benefit from the long-term experience of the expert Lidia Cánovas and gain a good overview on the important aspects that concern the structure and content of CTD Module 3.