Why CR Medicon

Service Platform

Regulatory Affairs

Industry's Leading CRO Company in Quality Standards

CR Medicon’s Regulatory & Registration Team is led by our industry experts, each with more than 18 years of experience

Medical Affairs

Medical Affairs

Based on the rich medical background and experience of our medical experts and medical writers

Biopharmaceuticals

Drug Clinical Monitoring And Project Management

CR Medicon’s clinical operations service has a staff of nearly 50 and continues to expand rapidly

Medical Devices

medical device

In China, clinical trials of medical devices and diagnostic reagents have certain specificities under

Biometrics

Data Management

From quality standard, industry experience in both US and China, to use of multiple EDC systems, CR Medicon’s data

Bioanalytical Lab Testing

bioanalysis

CR Medicon heavily invested and established in China a state-of-the-art biological sample analysis laboratory

Pharmacovigilance

Pharmacovigilence

CR Medicon team provides advanced pharmacovigilance solutions. We provide IND-filing needed information

Training

training

All members of CR Medicon’s expertise team are top experts in the industry. We have rich industry experience

Solutions

New Drug Clinical Development Strategy

clinical trial shutter

For the clinical development of new drugs, it is particularly important to develop an overall clinical strategy, combining un-met medical needs and known treatments prior to First-in-Human. More…

US-China Dual Registration

US-China

The CR Medicon team has extensive experience with new drug regulatory policies in both China and the United States. We have already served multiple clients who have conducted synchronous clinical development in US and China. More…

New Drug Early Phase Development

early phase

By integrating resources such as registration, medical, Phase I center, and PK testing lab, CR Medicon is able to complete high-quality new drug early phase research. More…

Proof of Concept & Pivotal

POC and Pivotal Clinical Research

Design and implementation of proof-of-concept and pivotal clinical research rely on high-level statistical and medical experts as well as an efficient and stable clinical operations team. CR Medicon has integrated key resources to fully support such projects. More…

Medical Device Clinical Research

medical device

CR Medicon established a dedicated medical device team, for better serving clients in medical device and IVD sectors. More…

Bioequivalence Test

Bioequivalence

CR Medicon has created an integrated bioequivalence test platform to help our clients achieve rapid development. More…

Client Success

We have successfully completed client projects in ...

PHASES

Bioequivalence
Phase I
Phase II
Phase III
IV/RWS
NDA

THERAPEUTIC AREAS

Oncology
Bioequivalence
Phase I Healthy Subject(PK/QTc/ADME)
Metabolic Disease
Infectious Disease
Immunology
Other

MARKETS

USA    
China

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