Mfds-Experienced CROs

Contract research organizations with Mfds regulatory submission experience

7 organizations

CJ HealthCare CRO

Clinical development arm of CJ HealthCare, providing Phase I-IV clinical trial management, BA/BE studies, and regulatory support services across South Korea with access to CJ's hospital network.

MFDS FDA

ClinTec International

Glasgow, United Kingdom Full Service

Glasgow-founded, India-expanded full-service CRO providing clinical trial management, site management, and regulatory services across Asia-Pacific, Europe, and North America.

FDA EMA PMDA TGA DCGI MFDS

Ildong Clinical Research

Seoul, South Korea Specialty

Clinical research division of South Korea's Ildong Pharmaceutical group, conducting domestic and international Phase I-IV studies with access to major Korean academic medical centres.

MFDS FDA

KCRN Research

Rockville, MD, USA Specialty

US-Korea bridge CRO providing early-phase clinical and regulatory services tailored for Korean life science companies entering the US FDA pathway.

FDA MFDS EMA

Korea United Pharm

Seoul, South Korea CDMO

Korean CDMO providing development and GMP manufacturing of solid oral dosage forms, injectables, and biosimilars, with FDA and EMA-inspected facilities serving global markets.

MFDS FDA EMA

Samsung Biologics

Incheon, South Korea CDMO

Leading CDMO providing end-to-end biopharmaceutical manufacturing services including cell line development, process development, and commercial manufacturing at massive scale.

FDA EMA PMDA MFDS

Symyoo

Seoul, South Korea Specialty

Seoul-based niche CRO specializing in dermatology and cosmetic clinical trials, providing IRB-approved study design, site management, and regulatory filing for K-beauty and pharmaceutical skincare products.

MFDS