Who We Serve

Pepgra has done extensive work in preparing PMS reports. Our PMS experts adhere to guidelines such as EMA, FDA, and other regulatory standards and protocols.

Our experts in regulatory affairs—from world’s top pharmaceutical firms—provide support for developing new medicinal products as well as integrating regulatory principles.

Our Clinical Research Associates are highly trained professionals who ensure integrity of the study and they are committed to excellence—on par with ICH & GCP standards.

Therapeutic capabilities play a pivotal role in organization’s success as a clinical research service provider. Pepgra has done holistic projects in the area of CRO therapeutics.