Clinical Trial Applications
(CTA)
Investigational New Drug (IND)

Clinical Trial Applications (CTA)
Investigational New Drug (IND)

BlueReg can prepare the entire documentation package required for your Clinical Trial Application/ Investigational New Drug Application (e.g: Investigators brochure, Investigational medicinal product dossier), compile the CTA/ IND, submit to the Competent Authorities and Independent Ethics Committees and liaise directly with CROs on your behalf.

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