| Clinical Research Services |
Triesta is a one step solution for oncology and oncology-related studies. We have a Central Ethics Committee for all our projects. The turnover time of this committee is 4-6 weeks. Since the committee is central, it saves time and makes work easier by acting as a one point link for all the HCG sites across the country.
Our Principal Investigators, CRCs, CRAs and the complete project teams are experienced and dedicated.click here
The wide array of services provided by these experienced workers are:
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1. |
Feasibility completion |
2. |
Investigator/site selection |
3. |
Assisting in pre-study qualification visits |
4. |
Assisting in study costing and budget preparations |
5. |
Organizing Ethics committee submissions and communications |
6. |
Provision of required study documents (financial disclosure, CVs, confirmation of adequate site facilities) |
7. |
Organizing Investigator meetings |
8. |
Recruitment and logistics planning and tracking |
9. |
Provision of study team at sites for trial conduct, documentation |
10. |
Record retention and archiving of study documentation |
11. |
Provision of facilities at site for conduct of research, and regular research related communication with sponsors and investigator’s team |
| 12 |
Assisting in study close out visits |
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1. |
Site initiation visits |
2. |
Interim site visits |
3. |
Close-out visits |
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1. |
Medical monitoring |
2. |
Safety reporting and medical review |
3. |
Preparation of SAE narratives and summaries |
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1. |
Protocol preparation |
2. |
CRF preparation |
3. |
Informed Consent Form preparation and review |
4. |
Informed Consent Form Translations |
5. |
Preparation of patient diaries |
6. |
Preparation of clinical study reports |
7. |
Preparation of abstracts and manuscripts |
8. |
Poster |
9. |
Full text articles |
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1. |
Collection and storage of biological sampl es |
2. |
Availability of biological samples for future rese arch |
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1. |
Receiving |
2. |
Storage |
3. |
Handling |
4. |
Dispensing |
5. |
Record Keeping |
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1. |
Provision and training of clinical research coordinators |
2. |
Protocol Training |
3. |
Process Training |
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Triesta encourages CROs and Sponsors to co-develop training modules and actively participate in training programs. |
| For more information about any of our services click here |
