Happy patient smiling — a representation of the human impact of clinical research

AI-Enabled Global Clinical Research Organization

Empowering Communities,Enriching Lives.

Clinical Research for Public Health.

At Proclin Research, it's personal. We deliver a level of collaboration and control not possible in a traditional CRO — guiding you successfully throughout your clinical development program.

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Our Manifesto

Guided by four principles that shape every trial we deliver.

01

Patient First

Every decision begins with the patient. Ethical, patient-centric conduct is the foundation of every trial we run.

02

Committed to Ethical Conduct

Integrity is non-negotiable. We uphold ICH-GCP, 21 CFR Part 11 and international confidentiality laws without compromise.

03

Access to New Medicine

We accelerate the path from protocol to patient, guiding sponsors successfully through clinical development.

04

Better Public Health

Our work exists to improve outcomes at scale — bringing quality research closer to the communities who need it.

What We Do

A full-service CRO, built for control and quality.

All Services

AI-Enabled Platform

A fully AI-enabled CRO — with compliance in place.

Our in-house CTMS, IWRS/RTSM and SMO tools run on a validated AI backbone — accelerating feasibility, monitoring and regulatory workflows for faster, more cost-efficient trials, without ever compromising on 21 CFR Part 11, GDPR or ICH-GCP.

AI Feasibility & Site Selection

Predictive models rank investigator sites on prior performance, patient pools and regional signals.

AI Risk-Based Monitoring

Machine learning flags outlier sites and data quality risks in real time inside our CTMS.

GenAI Protocol & Regulatory Assist

Accelerates protocol synopsis, informed consent drafting and DCGI / FDA submission narratives.

AI Chat Concierge

24×7 assistant answers sponsor and site questions across services and therapeutic areas.

Compliance by Design

Every AI workflow is validated against 21 CFR Part 11, GDPR and ICH-GCP — auditable end to end.

Unified Data Backbone

CTMS, IWRS/RTSM and EDC share a single, secure data spine for faster, cost-efficient trials.

Therapeutic Expertise

Ophthalmology — our flagship discipline.

From retinal disease and glaucoma to dry-eye programs, Proclin pairs decentralized imaging with tele-ophthalmology and central reading centers — widening access without compromising data integrity.

Infectious DiseaseOphthalmologyCardiologyNeurologyOncologyEndocrinology
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Ophthalmology examination

Global Reach

Local depth. Global scale.

With hubs across India and Europe and an expanding network of NABH and government hospital partners, Proclin delivers quality outcomes wherever your program needs to run.

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Clinical Trials Completed

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Continents — India & Europe

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Therapeutic Areas

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Compliance Commitment

AI, without compromise.

Every AI-enabled workflow — CTMS, IWRS, feasibility and monitoring — is validated against 21 CFR Part 11, GDPR, ICH-GCP and international confidentiality laws across India and Europe.

21 CFR Part 11GDPRICH-GCPDCGIUS FDA

Clearly Proclin

When you have clinical research questions, the answer is Clearly Proclin.

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