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Biopharma Dealmakers – What's an ECTD, and Why Should You Care?

13 July, 2016

Experienced biopharma dealmakers know that pharma companies seeking to partner with a biotech will require full disclosure of the regulatory submission documents. During due diligence, they will need to share the entirety of the IND or NDA with a potential partner. While many business development professionals may regard the internals of the IND or NDA as a huge black box of documents, regulatory professionals know this structure of documents inside the electronic submission is called an eCTD (electronic Common Technical Document).

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