Research Study Support and Coordination
One point of contact for your study, from design to final report.
Vsolv Research supports pharmaceutical and biomedical research studies from design to report. We plan the study, carry out or coordinate laboratory and in-vitro work, work with registered partner facilities where approvals are required, analyse the data and prepare the study report. Regulated studies involving humans or animals run only at facilities holding the required registrations and approvals.
Who it is for
- Companies needing laboratory or in-vitro studies for a product
- Startups without their own laboratory
- Researchers who need specific experiments or analysis
- Institutions coordinating multi-site work
What you receive
- Study design and protocol
- Laboratory and in-vitro work
- Coordination with registered partner facilities for studies that need approvals
- Data management and statistical analysis
- Study report with methods, results and raw data
- Support in preparing publications or regulatory summaries
How the work runs
- Consultation and NDA.
- Feasibility and study design.
- Protocol and approvals where required.
- Study conduct in-house or at partner facilities.
- Analysis and quality review.
- Final report and handover of data.
How fees are decided
Your fee depends on: study type and design · number of samples, groups or tests · analytical methods needed · partner facility charges · approvals and documentation · time frame.
You receive a written scope, agreed timeline and quote within 2 working days of your free consultation.
Scope and limits
Clinical studies need CDSCO approval where applicable, a registered ethics committee and CTRI registration; animal studies need a CCSEA-registered facility and institutional animal ethics approval. Such studies run only at facilities holding these registrations. We describe clearly which work is done in-house and which by partners.
Frequently asked questions
Do you conduct clinical trials?
No. We can help design studies and coordinate with registered sites and ethics committees, but trials run only at approved clinical sites.
Can you run animal studies?
Animal studies run only at CCSEA-registered facilities with institutional animal ethics approval. We can coordinate with such facilities.
Who owns the study data?
The client, on full payment, as set out in the contract. Raw data are handed over with the report.
Is my study kept confidential?
Yes. We sign an NDA before technical discussions and partner facilities are bound by confidentiality.
Last reviewed 27 September 2026.