clinical-trial-protocol
Draft a clinical trial protocol synopsis with the elements regulators and IRBs expect. Use when asked to write a clinical trial protocol, a study protocol synopsis, a trial design, or to structure endpoints/eligibility/statistics for an interventional study. Produces a structured protocol synopsis โ objectives, design, population with eligibility, interventions, endpoints, statistics, and safety/ethics โ for expert review. (For non-clinical/UX research, use research-protocol.)
Source facts
- Repository
- mohitagw15856/pm-claude-skills
- Last source activity
- July 14, 2026 at 12:39
- Detected SKILL.md language
- English
- Stars
- 1,261
- Forks
- 226
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