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.
   


 
ADVANTAGES AT CLINFOUND
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.
Chennal Buildings,
Kumaramangalam P O
Thodupuzha, Kerala-685 597
India
Tel: +91-484-6007955
Mob: +91 999 534 2978