We have extensive in-house clinical project management experience, good cooperation relationships with hospitals, and widely distributed offices. Besides ensuring smooth collaboration and transitioning of projects we participate in, we also optimize the duration of clinical trials and shorten the time to market of your drug product.
- Preparation of fundamental clinical trial documents (study protocol, case report form (CRF), informed consent, etc.)
- Clinical trial start-up (selecting principal investigator, clinical site, investigator meeting, ethics committee declaration, clinical site contracting)
- Clinical trial monitoring
- Clinical trial management
- Clinical trial audit and quality control
- Clinical trial summary report writing
- Medical affairs and pharmacovigilance