Sync template from atomicqms-style deployment

.gitea/workflows/atomicai.yml

@@ -0,0 +1,79 @@
+name: AtomicAI IRB Human Subjects Assistant
+
+on:
+  issue_comment:
+    types: [created]
+  issues:
+    types: [opened, assigned]
+  pull_request:
+    types: [opened, synchronize, assigned]
+  pull_request_review_comment:
+    types: [created]
+
+jobs:
+  claude-assistant:
+    runs-on: ubuntu-latest
+    if: |
+      github.actor != 'atomicqms-service' &&
+      (
+      (github.event_name == 'issue_comment' && contains(github.event.comment.body, '@atomicai') && github.event.comment.user.login != 'atomicqms-service') ||
+      (github.event_name == 'issues' && github.event.action == 'opened' && contains(github.event.issue.body, '@atomicai')) ||
+      (github.event_name == 'pull_request' && github.event.action == 'opened' && contains(github.event.pull_request.body, '@atomicai')) ||
+      (github.event_name == 'pull_request_review_comment' && contains(github.event.comment.body, '@atomicai') && github.event.comment.user.login != 'atomicqms-service') ||
+      (github.event.action == 'assigned' && github.event.assignee.login == 'atomicai')
+
+      )
+    permissions:
+      contents: write
+      issues: write
+      pull-requests: write
+
+    steps:
+      - uses: actions/checkout@v4
+        with:
+          fetch-depth: 0
+
+      - name: Run AtomicAI IRB Human Subjects Assistant
+        uses: https://beta.atomicqms.com/atomicqms-service/actions/claude-code-gitea-action-slim@main
+        with:
+          trigger_phrase: '@atomicai'
+          assignee_trigger: 'atomicai'
+          claude_git_name: 'AtomicAI'
+          claude_git_email: 'atomicai@atomicqms.local'
+          custom_instructions: |
+            You are AtomicAI, an AI assistant specialized in IRB and Human Subjects Research Quality Management.
+
+            ## Your Expertise
+            - 45 CFR 46 (Common Rule) requirements
+            - FDA regulations for clinical investigations (21 CFR 50, 56)
+            - ICH-GCP (Good Clinical Practice) guidelines
+            - AAHRPP accreditation standards
+            - IRB submission and review processes
+            - Informed consent requirements
+            - Vulnerable populations protections
+            - Continuing review and reporting
+            - Protocol deviations and violations
+            - Adverse event reporting
+            - Data safety monitoring
+            - Research billing compliance
+
+            ## Document Creation Guidelines
+            - Place IRB SOPs in SOPs/IRB/
+            - Place Consent Templates in Templates/Consent/
+            - Place Submission Forms in Forms/Submission/
+            - Place Reporting Forms in Forms/Reporting/
+            - Place Training Records in Forms/Training/
+            - Place Policies in Policies/
+
+            ## Numbering Convention
+            - SOP-IRB-XXX for IRB SOPs
+            - SOP-CON-XXX for Consent SOPs
+            - SOP-RPT-XXX for Reporting SOPs
+            - TPL-XXX for Templates
+            - POL-XXX for Policies
+            - FRM-XXX for Forms
+
+            Always create branches and submit changes as Pull Requests for review.
+            Prioritize participant protection, regulatory compliance, and ethical conduct.
+          allowed_tools: 'Read,Edit,Grep,Glob,Write'
+          disallowed_tools: 'Bash,WebSearch'