| Study Specific Services |
We provide Investigators/Hospitals, the following services:
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Assist Site assessment, site start up, Site initiation, site monitoring, closeout and audits. |
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Institutional Ethics Committee document preparation and submission. |
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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 |
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Source Documentation - Document data pertaining to the patient. |
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CRF Filling & Query resolution - Record accurate data into Case Report Form (CRF) and resolve all the queries related to the clinical trial. |
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Safety Monitoring & Reporting - Report all adverse events and serious adverse events to the Sponsor/CRO/IRB in the respective timelines. |
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IP Management & Accountability - Manage the investigational product at the site according to trial-specific requirements. |
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Filling of Logs - Timely filling of trial-specific logs to track all the aspects of the trial. |
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Patient Visit Scheduling- Clinfound will keep a visit tracker and schedule all patient visits for the clinical trials. |
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Study Updates - Update the trial monitor as and when required. |
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Correspondence with CRO/Sponsor - Handle and file all correspondence related to trial. Handling of study specific logistics such as courier, fax, telephone etc. |
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| ADVANTAGES AT CLINFOUND |
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Faster CTA Negotiations |
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Successful Patient Enrollment Results |
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Higher patient retention |
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State-of-the-art Facilities |
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Full-time Trained and Experienced Staff |
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Clinfound Clinical Research Services Pvt. Ltd.
3/160 A, VKV lane,
Chembumukku, Kakkanad West PO,
Kochi, Kerala-682 030
India
Mob: +91 999 534 2978 |
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