- Years of operation
- 5+
- Therapeutic areas
- 15+
- Research staff
- 20+
- Completed projects
- 10+
The organisation
CliniSolutions is a Site Management Organisation: it makes investigator sites work for sponsors and contract research organisations. The engagement covers site identification and feasibility, project and finance management, regulatory services, and the training that keeps site staff current.
The work spans more than fifteen therapeutic areas, delivered by a team of clinical research associates, regulatory specialists, data managers and site coordinators operating from the group's Mumbai office.
What sponsors engage us for
Five services, one accountable site partner
- Site identification & feasibility
- An honest read on whether a protocol's eligibility criteria match the patients a site actually sees, whether the visit schedule is realistic, and what the site would need to deliver the timeline being asked of it.
- Project management
- Day-to-day running of the study at site level: enrolment tracked against target, visits scheduled, queries closed and sponsor milestones met.
- Regulatory services
- Preparation and tracking of regulatory dossiers and ethics committee submissions, including amendments through the life of the study.
- Finance management
- Budget negotiation, per-visit reconciliation and investigator payments, kept auditable against what was actually delivered.
- Training & internship
- Keeping site staff current on protocol, consent and documentation practice, and bringing new clinical research professionals through structured placements.
Study lifecycle
Feasibility through close-out
A study is documented as it happens rather than reconstructed before an audit. That discipline is the difference between a site that passes inspection and one that does not.
Feasibility
Protocol fit, eligible population and achievable timelines assessed before commitment.
Site selection
Investigator sites identified and qualified against the protocol's specific requirements.
Submissions
Regulatory dossiers and ethics committee filings prepared, submitted and tracked.
Recruitment
Enrolment planned and delivered against target, with screening tracked to protocol criteria.
Informed consent
Conducted as a documented conversation with time for questions — never a signature to be collected.
Monitoring
Source documents, case report forms and accountability records kept ready for sponsor visits and audits.
Close-out
Final queries resolved, records archived to retention requirements, site obligations formally discharged.
Placing a study
Talk to the site before you commit the protocol.
Feasibility is where a study is won or lost. CliniSolutions will tell you what a site can realistically enrol before anyone signs a timeline.
CliniSolutions SMO & Research Organisation
A Site Management Organisation running clinical studies at investigator sites end to end, aligned to ICH-GCP.
27A, Ground Floor, 1st Wadi, Dharavi, Mumbai – 400017