Our mission
To generate credible clinical evidence through ethical, participant-centred and scientifically rigorous research — helping new treatments reach patients sooner.
About Ethica Research
An ethics-first clinical research partner connecting sponsors, investigators and patients across India.
Our story
Research that respects the people behind the data
Ethica Research was founded on a simple belief: clinical research in India can be faster and more ethical at the same time. We are a clinical research and site management partner for sponsors, CROs and investigators who want studies run with care, transparency and rigour.
We bridge the gap between global protocols and local realities. Our people understand hospital workflows, ethics committee expectations, regulatory timelines and — most importantly — the patients who make research possible. That understanding helps us recruit the right participants, keep them engaged and deliver clean, reliable data.
Our team brings together clinical operations, regulatory and quality expertise to support studies across Phase I–IV, medical devices and real-world evidence programs.
Our vision
To be India's most trusted clinical research partner, recognised for the integrity of our data and the care we show every participant.
Our values
The principles behind every study we run
Integrity
We do what we say, document what we do and report honestly — even when the news is not good.
Participant welfare
Every decision starts with the safety, rights and dignity of the people who volunteer for research.
Scientific rigor
Protocols are followed precisely and data are captured accurately, because evidence must be trustworthy.
Accountability
We take ownership of timelines and outcomes and keep our partners informed at every step.
Quality & compliance
Inspection-ready, every day
Our quality management system is built on documented SOPs, role-based GCP training, internal audits, CAPA tracking and regular mock inspections. Every study is conducted under approval from registered ethics committees and the national regulator.
Explore our services- ICH-GCP E6(R3) aligned
- CDSCO · NDCT Rules 2019
- Ethics-committee approved studies
- Participant safety first
Ready to start your next study in India?
Share your protocol synopsis and we will return a site feasibility assessment and start-up plan — confidentially and within five business days.
- Confidential review under NDA
- Response within one business day
- Direct PI and site assessment