CPD Courses

Preparing Submissions in the Common Technical Document (CTD) Format

Online Course grapl

About the CPD course

The CTD is the internationally recognised standard format for submissions to medicines regulatory authorities. In the European Economic Area; the USA and Canada; the CTD; in its electronic format (eCTD); is mandatory for all applications for marketing approval and all subsequent related submissions. The CTD is accepted in many other countries; being mandatory for new prescription medicines in some. This module explains the rationale for the CTD and provides guidance on its structure and format and the ways in which it is used.

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grapl

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grapl

grapl is a UK based digital learning and development specialist, authoring and designing Zenosis® courses to provide an extensive eLearning library for the pharmaceutical, biotech and medicinal products sector. This learning can be delivered via the customers LMS, the grapl LMS or its social, knowledge and collaborative CloudRooms platform. Continuously updated to reflect regulatory changes, Zenosis® courses are trusted to educate their people by some of the worlds leading companies. 

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