[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M7AGFBCPCFDWB8GHCKTFQTAB":3,"skill-same:01M7AGFBCPCFDWB8GHCKTFQTAB":47},{"skillNo":4,"name":5,"nameZh":6,"description":7,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":16,"categories":17,"keywords":18,"publishedAt":19,"linkOnly":20,"markdownContent":21,"markdownBody":22,"frontMatter":23,"refName":24,"commitSha":25,"skillDirectory":26,"forksCount":27,"repositoryHtmlUrl":28,"repositoryHomepageUrl":6,"ownerHtmlUrl":29,"ownerBlogUrl":30,"ownerDescription":31,"updatedAt":32,"install":33,"resources":46},"01M7AGFBCPCFDWB8GHCKTFQTAB","fda-qsr-audit-prep",null,"\u002Fcs:fda-qsr-audit-prep \u003Cscope> — FDA 21 CFR 820 (QSR \u002F QMSR) audit 6-question forcing interrogation. Post-Feb 2026 substantially harmonized with ISO 13485. Use before annual internal QSR audit, pre-FDA-inspection readiness, or Form 483 response.","Cyrilthetecchieee\u002Fcyril-code-","Cyrilthetecchieee","https:\u002F\u002Favatars.githubusercontent.com\u002Fu\u002F219787998?v=4","01M7AF0MMMKRAA0H61XMJPV92H","Julian Cyril D ","01M7AF0MQ10AVG6QJQ1C2BC0F5",2,"MIT","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fcompliance-os\u002Fskills\u002Ffda-qsr-audit-prep\u002FSKILL.md",[],[],"2026-11-15 14:19:17",false,"---\nname: \"fda-qsr-audit-prep\"\ndescription: \"\u002Fcs:fda-qsr-audit-prep \u003Cscope> — FDA 21 CFR 820 (QSR \u002F QMSR) audit 6-question forcing interrogation. Post-Feb 2026 substantially harmonized with ISO 13485. Use before annual internal QSR audit, pre-FDA-inspection readiness, or Form 483 response.\"\n---\n\n# \u002Fcs:fda-qsr-audit-prep — FDA QSR Forcing Questions\n\n**Command:** `\u002Fcs:fda-qsr-audit-prep \u003Cscope>`\n\nThe FDA QSR auditor pressure-tests any US medical-device QSR work. Six questions before any internal audit, FDA inspection, Form 483 response, or recall decision.\n\n## When to Run\n\n- Before annual internal QSR audit\n- Before pre-FDA-inspection readiness review (any device commercially distributed in US)\n- After receiving Form 483 observations\n- After Warning Letter receipt\n- After MDR-reportable event\n- Before recall decision (voluntary vs FDA-initiated)\n- Before submitting 510(k) \u002F PMA (where QSR posture affects approval timeline)\n\n## The Six QSR Questions\n\n### 1. Show me the complaint files from the last quarter — and the corresponding MDR reports.\n**21 CFR 820.198 + 21 CFR 803 — most-cited FDA inspection area.**\n- Complaint log complete: who \u002F what \u002F when \u002F device \u002F batch\n- Investigation closure within reasonable timeline\n- MDR-reporting decision tree applied: death OR serious injury OR malfunction-that-could-cause = MDR\n- 30-day timeline for most MDR reports; 5 days for certain serious events\n- Complaint trending input to management review\n\n### 2. When was process validation (IQ\u002FOQ\u002FPQ) last revalidated per 21 CFR 820.75?\n**Cross-walks ISO 13485 Clause 7.5.6 (substantially harmonized post-Feb 2026).**\n- Initial validation at process introduction\n- Revalidation triggers: process \u002F equipment \u002F material change OR periodic schedule\n- Statistical techniques per 21 CFR 820.250 where applicable\n- Cross-check with cs-cqm-iso13485 for ISO 13485 alignment\n\n### 3. Show me the DHRs for products commercially distributed in last 2 years.\n**21 CFR 820.180 — 2-year retention from commercial distribution; check sampling for completeness.**\n- Device History Record (DHR) for each unit\u002Flot\u002Fbatch\n- Must include: dates of manufacture, quantity manufactured, quantity released, acceptance records, primary identification label, device identification, control number\n- Sample stratified by product class\n- Verify DHR closeness to DHF (design history file)\n\n### 4. Show me CAPAs from the last 6 months with effectiveness verification.\n**21 CFR 820.100 = ISO 13485 8.5.2 substantially harmonized.**\n- Root cause analysis depth (5 Why minimum)\n- Effectiveness verification = measurable evidence, not \"we updated the procedure\"\n- Containment \u002F correction \u002F corrective action distinction documented\n- Closure approval by appropriate authority\n- Aging CAPAs > 90 days flagged\n\n### 5. Show me labeling (21 CFR 801) review for the most recent product launch.\n**FDA-specific overlay not in ISO 13485.**\n- Labeling per 21 CFR 801 requirements\n- For specific device types: also 21 CFR 800 series sectoral overlays\n- UDI (Unique Device Identification) per 21 CFR 830\n- Promotional materials reviewed for accuracy + non-misleading\n\n### 6. If a Form 483 was issued in the last 3 years, show me the closure status.\n**Form 483 = FDA observation; not equivalent to ISO nonconformity.**\n- Response within 15 working days\n- Each observation has documented corrective + preventive action with timeline\n- Effectiveness verification evidence\n- For Warning Letters: separate response track + potentially FDA meeting\n\n## Workflow\n\n```bash\n# 1. QSR compliance posture\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Fqsr_compliance_checker.py compliance_state.json\n\n# 2. FDA submission tracking (510(k) \u002F PMA \u002F IDE)\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Ffda_submission_tracker.py submissions.json\n\n# 3. HIPAA overlap (if connected device handles PHI)\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Fhipaa_risk_assessment.py phi_inventory.json\n\n# 4. Mock FDA inspection\npython ..\u002F..\u002Fskills\u002Fcompliance-os\u002Fscripts\u002Faudit_simulator.py fda_qsr_scope.json\n```\n\n## Output Format\n\n```markdown\n# FDA QSR Audit Prep: \u003Cscope>\n**Date:** YYYY-MM-DD\n\n## The Decision Being Made\n[programme-plan | inspection-readiness | 483-response | MDR-decision | recall]\n\n## Complaint + MDR Posture\n- Complaints last quarter: N\n- MDR-reportable events: M\n- MDR reports filed within timeline: % (target 100%)\n- Complaint trending review at management level: yes\u002Fno\n\n## Process Validation Status (21 CFR 820.75)\n- Validations on schedule: %\n- Stale validations: \u003Clist>\n- Statistical techniques applied: yes\u002Fno per process\n\n## DHR Completeness (21 CFR 820.180)\n- DHRs sampled: N\n- Completeness rate: %\n- 2-year retention compliant: yes\u002Fno\n- Stratified by product class: yes\u002Fno\n\n## CAPA Health (21 CFR 820.100)\n- CAPAs sampled: N\n- Root cause analysis depth: adequate\u002Finadequate\n- Effectiveness verification: complete\u002Fincomplete\n- Aging CAPAs > 90 days: N\n\n## Labeling (21 CFR 801)\n- Recent products reviewed: \u003Clist>\n- Labeling accurate + non-misleading: yes\u002Fno\n- UDI compliance per 21 CFR 830: yes\u002Fno\n\n## Form 483 \u002F Warning Letter History\n- Form 483s last 3 years: N (each: closed\u002Fin-progress)\n- Warning Letters last 5 years: N (each: closed\u002Fin-progress)\n- Pattern across observations: \u003Cthematic>\n\n## ISO 13485 Cross-Walk (post-Feb 2026 harmonization)\n- ISO 13485 audit findings: \u003Clink to cs-cqm-iso13485 output>\n- FDA-specific overlays remaining: labeling + complaint handling + MDR reporting + recall procedures\n- Cross-framework reuse: % of evidence shared\n\n## Verdict\n🟢 INSPECTION-READY | 🟡 GAPS-IDENTIFIED | 🔴 NOT-READY\n\n## Top 3 Actions\n[3 concrete next steps with owner + FDA-cited timeline (15 days \u002F 30 days \u002F etc.)]\n\n## Outside Counsel Required\n[For Warning Letter response, recall decisions, or 510(k) \u002F PMA strategy disputes]\n```\n\n## Routing\n\n- `\u002Fcs:compliance-readiness` — for multi-framework view\n- `\u002Fcs:iso13485-audit-prep` — for ISO 13485 cross-walk pair (substantially harmonized)\n- `\u002Fcs:gdpr-audit-prep` — if connected device handles personal data\n- `\u002Fcs:gc-review` — for Warning Letter response coordination\n\n## Related\n\n- Agent: [`cs-fda-qsr-auditor`](..\u002F..\u002Fagents\u002Fcs-fda-qsr-auditor.md)\n- Skill: [`fda-consultant-specialist`](..\u002F..\u002F..\u002Fra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002FSKILL.md)\n- Adjacent: `..\u002Fiso13485-audit-prep\u002F`, `..\u002Fcompliance-readiness\u002F`\n\n---\n\n**Version:** 1.0.0\n","# \u002Fcs:fda-qsr-audit-prep — FDA QSR Forcing Questions\n\n**Command:** `\u002Fcs:fda-qsr-audit-prep \u003Cscope>`\n\nThe FDA QSR auditor pressure-tests any US medical-device QSR work. Six questions before any internal audit, FDA inspection, Form 483 response, or recall decision.\n\n## When to Run\n\n- Before annual internal QSR audit\n- Before pre-FDA-inspection readiness review (any device commercially distributed in US)\n- After receiving Form 483 observations\n- After Warning Letter receipt\n- After MDR-reportable event\n- Before recall decision (voluntary vs FDA-initiated)\n- Before submitting 510(k) \u002F PMA (where QSR posture affects approval timeline)\n\n## The Six QSR Questions\n\n### 1. Show me the complaint files from the last quarter — and the corresponding MDR reports.\n**21 CFR 820.198 + 21 CFR 803 — most-cited FDA inspection area.**\n- Complaint log complete: who \u002F what \u002F when \u002F device \u002F batch\n- Investigation closure within reasonable timeline\n- MDR-reporting decision tree applied: death OR serious injury OR malfunction-that-could-cause = MDR\n- 30-day timeline for most MDR reports; 5 days for certain serious events\n- Complaint trending input to management review\n\n### 2. When was process validation (IQ\u002FOQ\u002FPQ) last revalidated per 21 CFR 820.75?\n**Cross-walks ISO 13485 Clause 7.5.6 (substantially harmonized post-Feb 2026).**\n- Initial validation at process introduction\n- Revalidation triggers: process \u002F equipment \u002F material change OR periodic schedule\n- Statistical techniques per 21 CFR 820.250 where applicable\n- Cross-check with cs-cqm-iso13485 for ISO 13485 alignment\n\n### 3. Show me the DHRs for products commercially distributed in last 2 years.\n**21 CFR 820.180 — 2-year retention from commercial distribution; check sampling for completeness.**\n- Device History Record (DHR) for each unit\u002Flot\u002Fbatch\n- Must include: dates of manufacture, quantity manufactured, quantity released, acceptance records, primary identification label, device identification, control number\n- Sample stratified by product class\n- Verify DHR closeness to DHF (design history file)\n\n### 4. Show me CAPAs from the last 6 months with effectiveness verification.\n**21 CFR 820.100 = ISO 13485 8.5.2 substantially harmonized.**\n- Root cause analysis depth (5 Why minimum)\n- Effectiveness verification = measurable evidence, not \"we updated the procedure\"\n- Containment \u002F correction \u002F corrective action distinction documented\n- Closure approval by appropriate authority\n- Aging CAPAs > 90 days flagged\n\n### 5. Show me labeling (21 CFR 801) review for the most recent product launch.\n**FDA-specific overlay not in ISO 13485.**\n- Labeling per 21 CFR 801 requirements\n- For specific device types: also 21 CFR 800 series sectoral overlays\n- UDI (Unique Device Identification) per 21 CFR 830\n- Promotional materials reviewed for accuracy + non-misleading\n\n### 6. If a Form 483 was issued in the last 3 years, show me the closure status.\n**Form 483 = FDA observation; not equivalent to ISO nonconformity.**\n- Response within 15 working days\n- Each observation has documented corrective + preventive action with timeline\n- Effectiveness verification evidence\n- For Warning Letters: separate response track + potentially FDA meeting\n\n## Workflow\n\n```bash\n# 1. QSR compliance posture\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Fqsr_compliance_checker.py compliance_state.json\n\n# 2. FDA submission tracking (510(k) \u002F PMA \u002F IDE)\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Ffda_submission_tracker.py submissions.json\n\n# 3. HIPAA overlap (if connected device handles PHI)\npython ra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002Fscripts\u002Fhipaa_risk_assessment.py phi_inventory.json\n\n# 4. Mock FDA inspection\npython ..\u002F..\u002Fskills\u002Fcompliance-os\u002Fscripts\u002Faudit_simulator.py fda_qsr_scope.json\n```\n\n## Output Format\n\n```markdown\n# FDA QSR Audit Prep: \u003Cscope>\n**Date:** YYYY-MM-DD\n\n## The Decision Being Made\n[programme-plan | inspection-readiness | 483-response | MDR-decision | recall]\n\n## Complaint + MDR Posture\n- Complaints last quarter: N\n- MDR-reportable events: M\n- MDR reports filed within timeline: % (target 100%)\n- Complaint trending review at management level: yes\u002Fno\n\n## Process Validation Status (21 CFR 820.75)\n- Validations on schedule: %\n- Stale validations: \u003Clist>\n- Statistical techniques applied: yes\u002Fno per process\n\n## DHR Completeness (21 CFR 820.180)\n- DHRs sampled: N\n- Completeness rate: %\n- 2-year retention compliant: yes\u002Fno\n- Stratified by product class: yes\u002Fno\n\n## CAPA Health (21 CFR 820.100)\n- CAPAs sampled: N\n- Root cause analysis depth: adequate\u002Finadequate\n- Effectiveness verification: complete\u002Fincomplete\n- Aging CAPAs > 90 days: N\n\n## Labeling (21 CFR 801)\n- Recent products reviewed: \u003Clist>\n- Labeling accurate + non-misleading: yes\u002Fno\n- UDI compliance per 21 CFR 830: yes\u002Fno\n\n## Form 483 \u002F Warning Letter History\n- Form 483s last 3 years: N (each: closed\u002Fin-progress)\n- Warning Letters last 5 years: N (each: closed\u002Fin-progress)\n- Pattern across observations: \u003Cthematic>\n\n## ISO 13485 Cross-Walk (post-Feb 2026 harmonization)\n- ISO 13485 audit findings: \u003Clink to cs-cqm-iso13485 output>\n- FDA-specific overlays remaining: labeling + complaint handling + MDR reporting + recall procedures\n- Cross-framework reuse: % of evidence shared\n\n## Verdict\n🟢 INSPECTION-READY | 🟡 GAPS-IDENTIFIED | 🔴 NOT-READY\n\n## Top 3 Actions\n[3 concrete next steps with owner + FDA-cited timeline (15 days \u002F 30 days \u002F etc.)]\n\n## Outside Counsel Required\n[For Warning Letter response, recall decisions, or 510(k) \u002F PMA strategy disputes]\n```\n\n## Routing\n\n- `\u002Fcs:compliance-readiness` — for multi-framework view\n- `\u002Fcs:iso13485-audit-prep` — for ISO 13485 cross-walk pair (substantially harmonized)\n- `\u002Fcs:gdpr-audit-prep` — if connected device handles personal data\n- `\u002Fcs:gc-review` — for Warning Letter response coordination\n\n## Related\n\n- Agent: [`cs-fda-qsr-auditor`](..\u002F..\u002Fagents\u002Fcs-fda-qsr-auditor.md)\n- Skill: [`fda-consultant-specialist`](..\u002F..\u002F..\u002Fra-qm-team\u002Fskills\u002Ffda-consultant-specialist\u002FSKILL.md)\n- Adjacent: `..\u002Fiso13485-audit-prep\u002F`, `..\u002Fcompliance-readiness\u002F`\n\n---\n\n**Version:** 1.0.0\n",{"name":5,"description":7},"main","57e7aa6b6e03bce1a7d7862ba9c2ec312f7f19b5","src\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fcompliance-os\u002Fskills\u002Ffda-qsr-audit-prep",0,"https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee","https:\u002F\u002Fwithcyril.me\u002F","Hi, I’m Julian Cyril D, a Computer Science and Business Systems student at PSNACET.\r\nI’m passionate about full-stack development, UI\u002FUX design, and building sma","2026-11-04 23:28:50",{"source":8,"skillName":5,"commands":34,"prompt":44,"zipAvailable":45},[35,38,41],{"tool":36,"command":37},"npx","npx skills add Cyrilthetecchieee\u002Fcyril-code- --skill fda-qsr-audit-prep",{"tool":39,"command":40},"bunx","bunx skills add Cyrilthetecchieee\u002Fcyril-code- --skill fda-qsr-audit-prep",{"tool":42,"command":43},"pnpm","pnpm dlx skills add Cyrilthetecchieee\u002Fcyril-code- --skill fda-qsr-audit-prep","安装技能，技能地址：https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fcompliance-os\u002Fskills\u002Ffda-qsr-audit-prep\u002FSKILL.md",true,[],[48,57,64,72,79,86],{"skillNo":49,"name":50,"nameZh":6,"description":51,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":52,"licenseFileUrl":53,"sourceHtmlUrl":54,"categories":55,"keywords":56,"publishedAt":19},"01M7AQV6CYX8RMC78420V9WZ62","webapp-testing","Toolkit for interacting with and testing local web applications using Playwright. Supports verifying frontend functionality, debugging UI behavior, capturing browser screenshots, and viewing browser logs.","Apache-2.0","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fwebapp-testing\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fwebapp-testing\u002FSKILL.md",[],[],{"skillNo":58,"name":59,"nameZh":6,"description":60,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":61,"categories":62,"keywords":63,"publishedAt":19},"01M7AQV2895N3S1MEX6K76G6G2","youtube-downloader","Download YouTube videos with customizable quality and format options. Use this skill when the user asks to download, save, or grab YouTube videos. Supports various quality settings (best, 1080p, 720p, 480p, 360p), multiple formats (mp4, webm, mkv), and audio-only downloads as MP3.","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fvideo-downloader\u002FSKILL.md",[],[],{"skillNo":65,"name":66,"nameZh":6,"description":67,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":52,"licenseFileUrl":68,"sourceHtmlUrl":69,"categories":70,"keywords":71,"publishedAt":19},"01M7AQTRNX62DNKVZ5GXEHRBKB","theme-factory","Toolkit for styling artifacts with a theme. These artifacts can be slides, docs, reportings, HTML landing pages, etc. There are 10 pre-set themes with colors\u002Ffonts that you can apply to any artifact that has been creating, or can generate a new theme on-the-fly.","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Ftheme-factory\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Ftheme-factory\u002FSKILL.md",[],[],{"skillNo":73,"name":74,"nameZh":6,"description":75,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":76,"categories":77,"keywords":78,"publishedAt":19},"01M7AQTNNVHAAN9H6DA8T6ZVE0","template-skill","Replace with description of the skill and when Claude should use it.","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Ftemplate-skill\u002FSKILL.md",[],[],{"skillNo":80,"name":81,"nameZh":6,"description":82,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":83,"categories":84,"keywords":85,"publishedAt":19},"01M7AQTJ3MQ6AKX152MEX2MYCC","tailored-resume-generator","Analyzes job descriptions and generates tailored resumes that highlight relevant experience, skills, and achievements to maximize interview chances","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Ftailored-resume-generator\u002FSKILL.md",[],[],{"skillNo":87,"name":88,"nameZh":6,"description":89,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":52,"licenseFileUrl":90,"sourceHtmlUrl":91,"categories":92,"keywords":93,"publishedAt":19},"01M7AQTD7D5MYET2YWG7HG9WM3","slack-gif-creator","Toolkit for creating animated GIFs optimized for Slack, with validators for size constraints and composable animation primitives. This skill applies when users request animated GIFs or emoji animations for Slack from descriptions like \"make me a GIF for Slack of X doing Y\".","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fslack-gif-creator\u002FLICENSE.txt","https:\u002F\u002Fgithub.com\u002FCyrilthetecchieee\u002Fcyril-code-\u002Fblob\u002Fmain\u002Fsrc\u002Fcyril_code\u002Fassets\u002F.skills_repo\u002Fslack-gif-creator\u002FSKILL.md",[],[]]