What we do

SERVICES

Management of Trial at Site

We strongly believe Clinical Research Coordinators play a vital role in bringing success by assisting the investigators in the preparation and conduct of the trials.

Oncquvia understands this & thus provides dedicated, full time and experienced CRCs to prioritize the work appropriately and be able to serve every trial related activity at the site.

         - Dedicated CRC at site

         - Back up CRC in case of absence of lead CRC

         - Full time GCP trained staff

SERVICES

Monitoring Services

We have a team of well-trained monitors having experience in Phase I and late Phase studies in various therapeutic areas. All our monitors adhere to high standards of quality which is our trademark.

SERVICES

Independent Quality Assurance/GCP Auditing

Our Audit team comprises of well experienced QA Auditors and GCP trained Medicos

SERVICES

Services during trial

Training at Sites

We provide training periodically /  at sites at regular intervals

01

ICH-GCP

02

Study Specific

03

Patient Recruitment & Retention