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IND Module 3
Hands-on Workshop

Start writing your Module 3 before its on the critical path!

Module 3 is the common template for Quality and CMC in Regulatory Submissions

When and where is it relevant?

Module 3 is relevant for all stages of development.

It is needed officially when submitting the first IND or IMPD, to initiate clinical trials, and serves all the way through to marekting applications (NDA or BLA in the US, MAA in Europe, and all major authorities worldwide).

Who should write it?

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Presented by Tamala Francis,
Founder & CEO at Francis & Co.

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In this workshop we will:

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