Services
Clinical research services
Everything you need to run a compliant, on-time study in India, delivered as a full service or function by function.
Clinical Operations
End-to-end trial management or stand-alone functions alongside your team.
Learn more →Site Management (SMO)
Trained study coordinators who keep sites enrolling, compliant and audit-ready.
Learn more →Regulatory Affairs
CDSCO, CTRI and ethics committee approvals handled by people who do it every week.
Learn more →Data Management & Biostatistics
21 CFR Part 11 compliant data management, statistics and medical writing.
Learn more →Pharmacovigilance
Safety monitoring and expedited AE/SAE reporting that keeps patients and studies safe.
Learn more →Quality Assurance
GCP audits, SOPs and inspection readiness from study start to database lock.
Learn more →Nutraceutical, Herbal & Cosmetic
Specialist studies that turn product claims into clinical evidence.
Learn more →Pre-Clinical Studies
Pharmacology, DMPK, toxicology and bio-analysis to take candidates into the clinic.
Learn more →How we work with you
Two ways to engage
Full service
ACRS runs your study in India end to end, from feasibility and approvals to the clinical study report, with one project manager accountable throughout.
Functional service provider
Bring us in for specific functions, such as monitoring, site management, data management or regulatory, to complement your own team or your global CRO.
Planning a study?
Tell us about your protocol, timelines and therapeutic area, and we will suggest how ACRS can support it.