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

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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Industry News & Updates

CR Medicon is a leader in CRO and an active contributor to our community and industry events.

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