; e-Learning: CTD Module 3
2021-11-30 2021-11-30 , Online Online, 390,- € plus tax Lidia Cánovas https://www.forum-institut.com/seminar/21122456-e-learning-ctd-module-3/referenten/21/21_12/21122456-e-learning-ctd-module-3_cnovas-lidia.jpg e-Learning: CTD Module 3

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

Topics
  • CTD structure and applicable guidelines
  • Drug substance Part
  • ASMF and CEP
  • Drug product part
Aims and objectives
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 programme.
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.
Who should attend

This e-Learning programme 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.

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

Webcode 21122456

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JETZT Buchen

Speaker


Everything at a glance

Appointment

anytime

anytime

Period

Venue

Online

Online

Fee
Ihr Ansprechpartner

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.

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

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 programme.
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.

Who should attend

This e-Learning programme 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.

Program

Module 1: Introduction
  • CTD Module 3 structure
  • Applicable guidelines
After having passed this section you know the structure of CTD Module 3 as well as essential quality guidelines.

Module 2: Drug substance part
  • CTD Module 3 drug substance data requirements
After having passed this module you are familiar with the subchapters of the drug substance part 3.2.S and the detailed data requirements.

Module 3: ASMF and CEP
  • Application and use
  • Structure
  • Procedure
After having passed this module you know the roles of the ASMF and CEP and when they are used.

Module 4: Drug product part
  • CTD Module 3 drug product data requirements
  • Appendices and regional information
After having passed this module you are familiar with the chapters and subchapters of the drug substance part 3.2.P and the data requirements, the information that should be included in the appendices and the regional information.

Trailer

e-Learning: CTD Module 3

Here you can get a brief insight into the e-Learning CTD Module 3.

Principles

Principles

The 'CTD Module 3' e-learning programme comprises four didactic modules that include videos in which expert Lidia Cánovas shares her expertise with you. You can also download and print the corresponding presentation documents. Each module also includes additional documents (links, guideline texts, etc.). The e-learning ends with an online test, which helps you practise and apply your newly gained knowledge. Once you have completed the four modules and passed the test, you will be awarded a certificate, which you can print out directly. The e-learning programme should be completed within three months.

How does it work?

1. Register for an e-learning programme on our website. 2. You will receive an email with your login data for access to our learning platform. 3. Log in to start your e-learning programme. 4. Complete the modules at your own pace. 5. Complete a multiple-choice test. 6. Once you have passed the test, you will be awarded a certificate, which you can then print out. Try out the demo versions of our e-learning programmes to get an idea of our learning environment.

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