About

Your partner in ethical and innovative clinical trials!

Who we are

Clinical Research, Redefined through Science, Ethics, and Speed.

At IRENEMEDS, we make complex clinical trials simple. As a full-service CRO, we partner with pharma, biotech, and nutraceutical companies to accelerate drug development—without compromising quality, compliance, or care.
Our Vision

Accelerating access to safe and effective therapies through ethical and innovation driven clinical research & rigorous marketing strategies.

Our Mission

Delivering clinical research solutions that guide sponsors from Concept → Clinic → Market, ensuring data quality, patient safety and regulatory compliance.

Our Motto

Driven by science. Guided by integrity. Focused on impact.

Science-Led

Innovation and evidence-based practices at the core.

Ethics-Focused

Upholding ICH-GCP and local regulatory standards with transparent communication.

Quality-oriented

SOP-driven processes and audit-ready documentation.

Innovation-Driven

Leveraging technology to make clinical development faster and smarter.

Your Trusted Partner in Global Clinical Innovation
At IRENEMEDS, we help bring breakthrough therapies to life—faster, safer, and smarter. As a full-service CRO, we blend scientific expertise with ethical rigor to transform global healthcare.
Leadership

Driving Innovation with Integrity and Expertise

At IRENEMEDS, leadership means blending scientific excellence with ethical responsibility. Our experienced team leads the way in redefining clinical research — ensuring every project advances with precision, transparency, and purpose.

Dr. Ruchika Irene Dillu

Founder & CEO, IRENEMEDS Private Limited
A seasoned physician-scientist with over 15 years of experience at the intersection of clinical medicine, pharmacology, and strategic leadership. Dr. Dillu holds an MBBS, MD in Pharmacology, and an MBA, combining deep scientific expertise with business acumen.

Dr. Vikram Rana

Co-Founder, IRENEMEDS Private Limited
Our Process

How We Bring Research to Life

Define the Strategy

We align on trial goals, regulatory pathways, and study design to lay the right foundation.

Execute the Study

From site setup to patient recruitment and monitoring—we manage it all with precision.

Analyze & Report

We handle data, stats, and regulatory-ready reporting to ensure audit-ready outcomes.

Support Post-Study

From regulatory submissions to market strategy, we stay with you beyond the trial.