What we do
- We identify potential sites
- Conduct the site selection as per the global clinical trial requirement
- Conduct a Pre-site selection visit & prepare a full database of site
- Assure quality data and on-time deliverables
- Provide operational management for domestic and international clinical trial programs
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
- A Data/ Site Manager is assigned to each study
- By providing a dedicated Clinical Research Coordinator, We;
- Save time
- Fasten patient recruitment
- Prevent loss to follow up & missed visits
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.
- Monitoring during all phases of a trial
- Site initiation
- Site management
- Telephonic monitoring between visits
- Presentations at monitoring visits- Training of site staff for ongoing support
- Site close-out
Independent Quality Assurance/GCP Auditing
Our Audit team comprises of well experienced QA Auditors and GCP trained Medicos
- Responsibilities of Audit team :
- Conduct independent audits at investigational sites
- Provide timely & comprehensive audit reports
- Mediate corrective actions as appropriate
Services during trial
- Assist in ICF process, screening and enrollment
- Coordinate subject follow up visits
- Manage drug accountability and distribution
- Coordinate central lab logistics and sample flow
- Coordinate monitoring and audit visits
- Subject reimbursements
- Maintain and update Site master file
- Coordinate SAE reporting on time
Training at Sites
We provide training periodically / at sites at regular intervals