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| Home >Why Triesta |
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| Client Friendly |
| A friendly project associate is your one point contact to solve all your queries related to laboratory, PET, bio-Repository, sites, investigators, recruitment etc. Our clients save valuable time during each stage of their project. |
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1. Triesta is experienced in all the phases of clinical trials, initial feasibility studies, and site management ranging from site selection to site training and closeout visits.
2. Medical Writing at Triesta comprises of protocol development, writing and managing clinical study reports, and serious adverse event reporting.
3. Triesta has a state of art Bio-repository operational under stringent guidelines and well laid down processes and SOPs.
4. A state of art Laboratory with latest in oncology diagnosis is another hallmark of Triesta.
5. Triesta has carved a niche for itself in biomarker research in the field of cancer. |
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| Triesta believes in timely delivery of consistent, accurate, high quality, precise and correct scientific data. |
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Our Board of Directors, Clinical Advisors, Consultants, Lab technicians, Pathologists, Imaging Experts, Clinical Research Associates and Coordinators, and Medical Writers have extensive clinical research experience in oncology. |
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Our Board of Directors, Clinical Advisors, Consultants, Lab technicians, Pathologists, Imaging Experts, Clinical Research Associates and Coordinators, and Medical Writers have extensive clinical research experience in oncology. |
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We work closely with several leading hospitals and medical institutions within India for our research. HCG is the largest network of oncology hospitals in South Asia. |
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Feasibilities studies are managed through one common contact at the central office. The executives provide you with feasibilities from the network across the country, within a pre-specified timeline. They help you select the appropriate investigators and sites for your studies. contact us |
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Our study start up specialists are in regular touch with you to assist you in all the visits, meetings and documentation prior to study start-up at each site. Irrespective of the number of network sites, we have a one point contact to help you organize your trial related process, throughout the network across the country. |
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We have access to a large database of cancer patients through our network for participation in our research studies. The recruitment teams at the site would work after study start up towards aggressive competent recruitment targets. Team of coordinators (both doctors and non-doctors) would work towards accurate documentation and assist you during monitoring visits. |
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Experienced Principal Investigators, a competent staff, stringent processes and ethics, competent medical facilities along with transparency in treatment enables us to retain patients in the clinical trials. |
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Our QA team assists you in ensuring timely processing of surplus clinical trial supplies and drugs at the end of the study, and archival of study related documents as per regulatory requirements. |
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