Service content：
We provide clinical trial services of various kinds of importd medical devices and indigenous medical devices,of which content involve: clinical package sevice,clinical protocol design,clinical supervising,clinical inspection,carrying out clinical researcher conferences,clinical consult,clinical data management and statistics,composing clinical research report and so on.We develop modularized service in accordance with clients'requirements. We provide one-step,all-around and comprehensive solutions.
Service process：
- Signing commission service contract
- Preparing essential clinical trial documents(protocol,case report,informed consent form and etc.)
- Starting clinical trial(researcher and selection of research center,organizing researcher conferences,declaring ethics,signing clinical research contract with research center,stc.)
- Supervising clinical trial
- Managing clinical trials
- Clinical trial safety report
- Supervising clinical trial and quality control
- Clinical data management and statistics analysis
- Composing final clinical trial report
Service introduction：
Trial period:
The exact trial period must be confirmed on the basis of product performance and characteristic.
Trial expense:
The expense is composed of research center charges and Hotwire charges.It depends on selection of institution and complexity of trials.