I will teach, write and register clinical trial for you

Being a health scientist, I have vast experience in conducting clinical trials. I can assist in

1. Designing Randomized Clinical Trials (RCTs) and Non-randomized Clinical Trials
2. Writing clinical trial protocols
3. Registering protocols of clinical trial at WHO-accredited clinical trial registries
4. Preparation of required documents for conducting clinical trials (consent forms, participant information sheets, and case report forms, specific documents for obtaining ethical approval from the ethics board etc.)
5. Conducting clinical trials
6. Statistical analysis of the clinical trial
7. Writing the trial report
8. Publishing the findings of the clinical trial
9. Training your team in conducting clinical trials
10. Other aspects related to clinical trials (regulatory requirements related to clinical trials, recruitment and retention of participants, randomization, blinding, placebo trials, and so on...)

To ensure high-quality, international guidelines such as SPIRIT Statement and CONSORT Guidelines will be followed.

I can also assist in conducting

• Systematic review and meta-analysis of clinical trials
• Risk of bias assessment/Quality assessment/ Critical appraisal of clinical trials