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clinical-protocol-author

Author a per-trial clinical protocol (background + design + endpoints + eligibility + treatment + safety monitoring + statistical analysis plan + ethics/regulatory). ICH-GCP E6(R3). FDA IND / EMA CTR submission-ready. Chief Medical Officer authored. Use when user asks to "draft a clinical protocol" or "create the clinical protocol". Do NOT use for "audit existing clinical protocol" (use clinical-protocol-audit instead).

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Source facts

Repository
cyberskill-official/cyberos
Last source activity
July 20, 2026 at 02:42
Detected SKILL.md language
English
Stars
60
Forks
2

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