Services
A full-service CRO, end to end.
From feasibility and site selection to regulatory submission and training — Proclin delivers collaboration and control across every phase of clinical development.
01 — Seamless end-to-end submissions
Monitoring & Regulatory
A full team of regulatory professionals handles DCGI, US FDA and international submissions, led by former regulatory authorities.
02 — MedTech, wearables and diagnostics
Devices & IVD
Medical device and In-Vitro Diagnostic (IVD) studies spanning clinical investigations, performance evaluations and CDSCO / FDA registration support.
03 — Advancing clinical research careers
Training & Development
Certified CRA and CRC programs advance careers with structured modules, assessments and robust placement assistance.
04 — AI-native trial management
In-house CTMS
Our proprietary Clinical Trial Management System unifies planning, monitoring, finance and documents on a single, 21 CFR Part 11-validated platform — with AI-driven insights baked in.
05 — Faster, smarter site selection
SMO & AI Feasibility
Our Site Management Organization combined with AI-powered feasibility tools accelerates site identification, patient prediction and study start-up — cutting time and cost.
06 — Faster trials, higher-quality data
Clinical Operations
Deeply experienced clinical teams execute and manage trials and observational studies across Phase I–IV with rigorous, patient-first conduct.
07 — A network built on trust
Site Partnership
Our Site Management Unit strengthens independent practices and hospital partners, blending experienced and young clinicians into high-performing teams.
08 — Dermatology-led consumer studies
Cosmetics
Dermatology-led cosmetic safety, tolerability and efficacy studies — patch testing, ophthalmic tolerance and consumer perception, with cruelty-free ethics.
09 — Randomization & supply, automated
IWRS / RTSM
Interactive Web Response System for randomization and trial supply management — configurable in days, not months, and integrated natively with our CTMS and EDC.
010 — Evidence for functional health
Nutraceutical Trials
Efficacy, safety and bioavailability studies for nutraceuticals, functional foods and dietary supplements — aligned with FSSAI, DCGI and global evidence standards.