Services: Ethic and Regulatory

Comprehensive Services

Ethic and Regulatory

Ethics Committee/IRB and Regulatory Authority Submission
Submission and Accelerating Approval letter

Clinical trial should be conducted in accordance with the ethical principles that have their origin in the Declaration of Helsinki and in compliance with protocol that has received Ethic Committee approval.
Prodia the CRO prepare any related documents and accelerate submission letter of approval from EC and regulatory (BPOM).