Study Specific Services

We provide Investigators/Hospitals, the following services:

Assist Site assessment, site start up, Site initiation, site monitoring, closeout and audits.
Institutional Ethics Committee document preparation and submission.
Informed Consent Form Process – Conduct informed consent sessions with the trial patient and explain the merits and demerits of the study and obtain the consent of the trial patient
Source Documentation - Document data pertaining to the patient.
CRF Filling & Query resolution - Record accurate data into Case Report Form (CRF) and resolve all the queries related to the clinical trial.
Safety Monitoring & Reporting - Report all adverse events and serious adverse events to the Sponsor/CRO/IRB in the respective timelines.
IP Management & Accountability - Manage the investigational product at the site according to trial-specific requirements.
Filling of Logs - Timely filling of trial-specific logs to track all the aspects of the trial.
Patient Visit Scheduling- Clinfound will keep a visit tracker and schedule all patient visits for the clinical trials.
Study Updates - Update the trial monitor as and when required.
Correspondence with CRO/Sponsor - Handle and file all correspondence related to trial. Handling of study specific logistics such as courier, fax, telephone etc.

Faster CTA Negotiations
Successful Patient Enrollment Results
Higher patient retention
State-of-the-art Facilities
Full-time Trained and Experienced Staff
Clinfound Clinical Research Services Pvt. Ltd.
3/160 A, VKV lane,
Chembumukku, Kakkanad West PO,
Kochi, Kerala-682 030
Mob: +91 999 534 2978