OUR COMPANY
ClinSite, a leading Contract Research Organisation (CRO) provides a unified platform to sponsors and Clinical Trial Sites to effectively execute and obtain credible clinical trial data across multiple therapeutic areas.
As a trusted partner in clinical research, we provide a comprehensive suite of services tailored to your specific needs, upholding the highest standards of quality and compliance.
Our project team brings over a decade of industry expertise on average, with extensive experience across various therapeutic fields.
Our competitively priced packages are designed to optimize the entire clinical trial process, delivering cost-effective, efficient, and successful outcomes.
Learn more about our CRO Services, SMO Services, and Functional Service Provider (FSP) solutions and discover how we can support the success of your clinical trials.
Our network of sites has been built on relationships, experience and knowledge of the sites’ capabilities.
ClinSite offers an end-to-end CRO services, standalone trial functions, or access to experienced clinical operations staff as needed, tailored to accommodate the specific needs of each client.
We advocate for a risk-based monitoring approach, enhancing the quality and effectiveness of clinical trials by assigning a dedicated project team.
- Highly experienced team
- Proven track record in conducting phase II-IV clinical trials
- Robust regulatory approvals
- Strong on ground presence
- Integrated clinical trial sites network
- Accurate and consistent documentation
- Identify and enrol right participants into each study
- Standardized SOPs for all sites
- Support our partner in audit/regulatory inspection
- Ensure the efficient and ethical conduct of trials
- Cost effective solutions
Network of Clinical Trial Sites
ClinSite has a integrated network of specialised and top enrollers – clinical trial sites (CTS) across various regions in the world. Our network sites have established the necessary infrastructure, human resources, and facilities to conduct research within these centres. All the sites are GCP-trained sites and strictly follow Good clinical practices that ensure the integrity and quality of the data produced in the clinical trials at optimal study speed.
Why choose ClinSite integrated network
- Access to large pool of participants
- Treatment-naïve patient populations
- Motivated Principal Investigators
- Proven track record
Our Solution for Sponsor, Site, Participant
Feasibilities
Through prequalified alliance site network. Our team will help you rapidly identify sites specifically qualified for your study
Clinical Trial Monitoring
Through a team of seasoned professionals ensuring the highest standards of quality and compliance throughout the duration of the trial
Regulatory Approvals
Through highly experienced professional ensuring expedited and fast pace approvals
Quality Assurance
Through a seasoned professional having vast & international experience of internal and external audits
Recruitment
Through collaboration with local community health centres, Government Institutes, doctors, clinics, and hospital database
Compliance
To study protocol through patient education, procedure for patient next visit reminders via dedicated follow-up team
Therapeutic Focus
Over 10 years of experience in participating in Phase II-IV clinical trials in a wide variety of therapeutic areas.
Oncology
Immunology
Endocrinology
Infectious Disease & Vaccines
Gastroenterology
Dermatology
Nutrition
Cardiology
Pain Management
Anesthesia & Critical Care
Ophthalmology
Pulmonology
Surgery
Paediatrics
Gynaecology
Request for Proposal
Submit your details and one of our experts will respond to you as soon as possible.
ClinSite is committed to protecting your privacy. By submitting this form, you confirm that you have read and agree to our privacy policy terms and conditions.
10+
Years of Research Experience
10+
30+
Sites in ClinSite Alliance Network
35000+
Participants Enrollement
80%
Exceed our Enrollment Goal
