We Serve

Pharmaceutical Companies

Medical Device Companies

Dietary Supplement Manufacturing Companies

Pharma Companies in Alternative Medicine

Who are we ?

We are Quest Clinical Services. We are SOP adhered India based Contract Research Organization. We deal and run the show with data, medical writing, good clinical practices, ethics committees, investigators and the subjects. We understand that you have good product with you. We will help you prove the same. Be it a drug, a nutraceutical, or a medical device, we are committed to provide customized solutions to our clinical partners from small and midsize companies to global pharma companies.

Our Services

Medical Writing and Biostatistics

Clinical trial begins with an idea. It is then germinated through writing! Synopsis, Protocol, Informed Consent Documents, Case Record Form and all such documents are drafted in-house of QCS.

Selection of PI and Site

If you have your list of sites and physicians, good, if not, it’s still okay. Depending on the need of the study, we will identify physicians, talk to them, train them the protocol and GCP and make them ready to undertake your trial!

Site Management

Clean, high-quality data is one of the most critical elements of any clinical trial. To accomplish the same, site management an important aspect.

Regulatory

QCS will help you submit the dossier to the DCGI. Specifically, QCS can assist you with the following activities:National Regulatory Services, GCP training

GCP training

QCS believes in continuous training and education, both internally, with our own team and externally with our clients. It not only is a regulatory requirement, but it also makes sure that everyone is on the same platform.

Therapeutic Expertise

India has a large and diverse patient pool in almost every therapeutic area. India has an added advantage in clinical research.