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This repository was archived by the owner on Mar 18, 2026. It is now read-only.
* Add prek git hooks
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Add prek.toml config
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Add lefthook commit-msg and pre-push hooks
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Complete lefthook to prek migration
Move commit-msg and pre-push hooks from lefthook.yml
into prek.toml as local shell hooks. Build prek from
source in flake.nix instead of using nixpkgs. Remove
lefthook from dev shell.
* Add prek CI workflow and document nix commands
Add GitHub Actions workflow using Determinate Nix to
run prek checks on push/PR. Document nix develop
commands in README.md and AGENTS.md.
* Fix beads-rust x86_64-linux hash for upstream tarball change
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Fix trailing whitespace and end-of-file issues
Auto-fixed by prek builtin hooks (trailing-whitespace,
end-of-file-fixer).
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Use self-hosted runner with fallback for prek CI
Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com>
* Trigger CI
---------
Co-authored-by: Claude Opus 4.6 <noreply@anthropic.com>
- Add missing dependencies with `bd dep add <child> <parent> --type blocks`
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-`bd blocked` should show tasks waiting on dependencies
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-`bd stats` should show accurate counts
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IMPORTANT: Plan only. Do NOT implement anything. Do NOT assume functionality is missing;
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IMPORTANT: Plan only. Do NOT implement anything. Do NOT assume functionality is missing;
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use `bd list` and code search to verify first.
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ULTIMATE GOAL: Refactor all knowledge-work plugins from generic Anthropic templates to FashionUnited-specific workflows, tools, and domain context. Ensure all necessary tasks exist as beads with proper dependencies so `bd ready` always shows the right next work.
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ULTIMATE GOAL: Refactor all knowledge-work plugins from generic Anthropic templates to FashionUnited-specific workflows, tools, and domain context. Ensure all necessary tasks exist as beads with proper dependencies so `bd ready` always shows the right next work.
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## License
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This fork is licensed under Apache 2.0, same as the [original Anthropic repository](https://github.com/anthropics/knowledge-work-plugins). See [LICENSE](LICENSE) for details.
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## Development Environment
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```bash
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nix develop # Enter dev shell with all tools
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nix develop --command prek run --all-files # Run pre-commit checks
Copy file name to clipboardExpand all lines: archived/bio-research/skills/clinical-trial-protocol/references/02-protocol-foundation.md
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**Content to Generate:**
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STATEMENT OF COMPLIANCE
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Provide a statement that the trial will be conducted in compliance with the protocol, International Conference on Harmonisation Good Clinical Practice (ICH GCP) and applicable state, local and federal regulatory requirements. Each engaged institution must have a current Federal-Wide Assurance (FWA) issued by the Office for Human Research Protections (OHRP) and must provide this protocol and the associated informed consent documents and recruitment materials for review and approval by an appropriate Institutional Review Board (IRB) or Ethics Committee (EC) registered with OHRP. Any amendments to the protocol or consent materials must also be approved before implementation. Select one of the two statements below:
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Provide a statement that the trial will be conducted in compliance with the protocol, International Conference on Harmonisation Good Clinical Practice (ICH GCP) and applicable state, local and federal regulatory requirements. Each engaged institution must have a current Federal-Wide Assurance (FWA) issued by the Office for Human Research Protections (OHRP) and must provide this protocol and the associated informed consent documents and recruitment materials for review and approval by an appropriate Institutional Review Board (IRB) or Ethics Committee (EC) registered with OHRP. Any amendments to the protocol or consent materials must also be approved before implementation. Select one of the two statements below:
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(1) [The trial will be carried out in accordance with International Conference on Harmonisation Good Clinical Practice (ICH GCP) and the following:
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(1) [The trial will be carried out in accordance with International Conference on Harmonisation Good Clinical Practice (ICH GCP) and the following:
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• United States (US) Code of Federal Regulations (CFR) applicable to clinical studies (45 CFR Part 46, 21 CFR Part 50, 21 CFR Part 56, 21 CFR Part 312, and/or 21 CFR Part 812)
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• United States (US) Code of Federal Regulations (CFR) applicable to clinical studies (45 CFR Part 46, 21 CFR Part 50, 21 CFR Part 56, 21 CFR Part 312, and/or 21 CFR Part 812)
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National Institutes of Health (NIH)-funded investigators and clinical trial site staff who are responsible for the conduct, management, or oversight of NIH-funded clinical trials have completed Human Subjects Protection and ICH GCP Training.
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#### Section 1.2: Schema (30 lines)
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**Generate a text-based flow diagram** showing study progression.
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**Generate a text-based flow diagram** showing study progression.
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**Required Elements:**
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-**Screening Period:** Show duration (e.g., "Within 28 days") and key activities (eligibility assessment)
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