Protocol/CRF development
StatPlus will collaborate with
investigators and clients in the protocol/CRF development to:
1. Develop protocol from scratch or refine the protocol template received from the client,Emphaome will be in the issues of study design Endpoint selection,patient selection,trial duration,sample size determination,and statistical analysis.The protocol will be local hospitals
- Meet the requirements of DOH and local hospitals
- Serve marketing purpose
- Demonstrate strong scientific base
- Minimize cost
2. Design CRFs based on
protocol to capture all necessary information specified by Protocol.3. Design informed consent
form
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