End-to-end clinical research solutions designed to accelerate your drug development program across India.
As a Site Management Organization, CliniSearch Associates provides comprehensive site management services from initial feasibility through study closeout. We act as the operational backbone for sponsors and CROs, ensuring smooth execution at every stage.
Our experienced team manages site operations, regulatory submissions, patient recruitment, monitoring support, and data quality — all under one roof.
Our data management team delivers accurate, timely, and ICH E6(R2)-compliant data management services. We support both paper-based and electronic CRF platforms with rigorous quality control processes.
With a focus on fast turnaround times and data integrity, our CDM services ensure your study database is clean, consistent, and audit-ready at all times.
CliniSearch Associates offers complete solutions for hospitals and institutions looking to establish, register, or maintain a fully compliant Independent Ethics Committee (IEC) under the DCGI regulatory framework.
Our team assists with IEC formation, regulatory registration, accreditation, and ongoing compliance management — ensuring your committee operates at the highest standards.
We assist hospitals in achieving and sustaining NABH (National Accreditation Board for Hospitals) accreditation standards. Our team works closely with hospital administration to implement quality systems and ensure day-to-day compliance.
From process optimization to staff training and documentation support, CliniSearch Associates is your trusted partner in hospital quality management.
Our facility management division offers comprehensive manpower and facility solutions for both healthcare and non-healthcare industries. We ensure your environment meets the highest standards of cleanliness, safety, and operational efficiency.
Our experts are ready to design a tailored solution for your clinical research program in India.