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2-Day Course: Common Technical Document (CTD) (London, United Kingdom - July 3-4, 2019) -

The "Common Technical Document" conference has been added to's offering.

Project management/collection of critical documents for chemistry, manufacturing and control (CMC) for global registration (CTD) and incorporate quality by design within the CTD

This two-day course will provide you with a clear understanding of the regulatory and technical requirements for CMC management of your full and generic application in major markets of EU and USA. Furthermore, the course examines the requirements for global roll out of the document to ROW regions including, LATAM, ASEAN, MENA and CIS territories.

You will increase your ability to manage all aspects of development of the CMC applications after two days of intensive lectures, group work, and discussion session, covering everything you need to know about compiling the chemistry and pharmacy section of your generic dossier.


Programme Day One

  • What is the CTD? The road map to Module 3 Understanding ICH
  • Assessing the impact of the harmonisation - ICH guidelines
  • Preparing the drug substance section of the application - US and EU
  • GMP for Active Substances
  • Case study - Essential information from API suppliers
  • Examining the content of the sections concerning the drug product - Composition and development of the drug product

Programme Day Two

  • Writing the section on manufacture of the drug product and process validation
  • Writing the sections on Excipients and Packaging Components
  • Writing the sections on control of the finished product and Case Study
  • Writing the stability section
  • The function and content of the Quality Overall Summary
  • Examining Global Roll-out of CTD - Module 3
  • Examining Change Control - Practical tips
  • Practical Exercise in Generic Development

For more information about this conference visit

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Last Updated: 04-Dec-2018