StatPlus collaborates with investigators and clients to develop protocols and CRFs for clinical trials.

Our services include:

1. Protocol Development:

• We can develop a protocol from scratch or refine a  protocol template received from the client. 

• We focus on study design, endpoint selection, patient  selection, trial duration, sample size determination, and  statistical analysis. 

• Our protocols are tailored to meet the requirements of DOH and local hospitals. 

• Our protocols serve a marketing purpose and demonstrate a strong scientific base. 

• We aim to minimize costs while ensuring the quality of the protocol.

2. CRF Design:

• We design CRFs based on the protocol to capture all necessary information specified by the protocol.

3. Informed Consent Form Design:

• We design informed consent forms to ensure that patients understand the study and their rights.