Medical Affairs

Medical Affairs

Based on the extensive medical background and experience of our medical experts and medical writers, CR Medicon Medical Affairs Service for our clients develops optimal clinical development plans, provides best-quality clinical trial design and draft as well as preparation of registration dossier. Our medical monitoring team focuses on medical monitoring services for clinical research and establishes the most professional and efficient medical monitoring system. CR Medicon's Pharmacovigilance team provides deep insights into clinical trial safety risks and provides high-quality pharmacovigilance solutions.


  • Develop Phase I-III clinical research strategies based on our internal professional statistical and PK expert resources
  • Provide medical writing services for, but not limited to , Phase I-III, BE Clinical Research Protocols, Investigator's Brochure (IB), Summary Report
  • Prepare preclinical package
  • Medical monitoring service


  • All of our team members have MD and medical master degrees. Furthermore, each core member has 10-20 years of experience in innovative drug development in both US and China.
  • Our team has successfully completed hundreds of Phase I-III clinical trial protocols that cover a wide range of disease categories.
  • Our team has published a number of research papers in well-known journals, both in China and around the world.