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!
Clean, high-quality data is one of the most critical elements of any clinical trial. To accomplish the same, site management an important aspect.
QCS will help you submit the dossier to the DCGI. Specifically, QCS can assist you with the following activities:National Regulatory Services, 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.
India has a large and diverse patient pool in almost every therapeutic area. India has an added advantage in clinical research.