Watch It Work
See how compliance training becomes FDA-compliant audit documentation instantly
FDA/ISO audits require documentation, not video files
FDA/ISO Compliance Features
Docsie generates compliant training documentation that meets FDA CFR 21 Part 11, ISO 13485, and GxP requirements—with audit trails, version control, and electronic signatures.
Electronic signatures, audit trails, and document control that meet FDA requirements for pharmaceutical and medical device training documentation
Auto-tag content by regulation (CFR 21 Part 11, ISO 13485, GxP, HIPAA). Auditors can search for specific compliance topics instantly
Complete document history showing what changed, who changed it, and when. Meets ISO/FDA requirements for document control and change management
Simple Process
Powered by Docsie Copilot's compliance-aware AI
Upload GMP training, SOP videos, or regulatory training from your LMS. Supports FDA-validated file formats
AI maps training to FDA/ISO regulations, creates version-controlled documentation with audit trails and electronic signature readiness
Get FDA CFR 21 Part 11-compliant documentation with audit trails, training completion records, and regulation references
Audit-ready deliverables from compliance training footage
Training documentation with electronic signature readiness, audit trails, and version control that meets FDA requirements for pharmaceutical and medical device industries
Training content automatically tagged to FDA regulations (CFR 21 Part 11, GMP), ISO standards (13485, 9001), and GxP requirements for instant audit evidence retrieval
Complete change history showing who trained, what changed, when it changed—with document control meeting FDA/ISO requirements for training record management
Employee training certificates with documented proof of GMP, GxP, or ISO training completion—timestamped records for regulatory inspections and audits
Find training on specific FDA regulations, SOPs, or quality procedures instantly—auditors search "CFR 21 Part 11" and get all related training documentation
Documentation organized by role and competency requirement—quality engineers get GMP docs, lab staff get GLP training, production staff get manufacturing procedures
Watch how Docsie analyzes GMP training videos and generates FDA CFR 21 Part 11-compliant documentation with audit trails and regulation mapping
No credit card required • 14-day free trial
Common Questions
Everything you need to know about video-to-documentation conversion
Q: How is this different from basic transcription tools?
A: Most tools only convert speech to text. Docsie's multimodal AI actually watches and analyzes the video content—reading on-screen text, identifying UI elements, detecting code in IDEs, capturing key visual moments, and correlating what's said with what's shown. It's the difference between having a typist versus having an intelligent analyst watch your video.
Q: What video formats are supported?
A: We support all major video formats including MP4, MOV, AVI, WebM, MKV, and more. You can also provide YouTube URLs or links to videos hosted on other platforms.
Q: How long does the conversion process take?
A: Processing time varies by video length, but typically runs at about 15-20% of the video duration. A 30-minute video is usually ready in 5-10 minutes.
Q: How accurate is the transcription and visual analysis?
A: Our AI achieves 95%+ accuracy with clear audio and technical content. The visual analysis (OCR, UI element detection, code recognition) is similarly accurate and trained specifically on technical content, IDEs, and documentation scenarios.
Q: Can I edit the generated documentation?
A: Absolutely! The AI-generated documentation serves as a solid first draft that you can edit, refine, and customize using Docsie's built-in editor. All formatting and structure is preserved.
Still have questions?
Book a DemoCompatible with major video platforms and formats
Process YouTube videos and playlists
Convert Vimeo content
Convert Loom recordings
Support for MP4, AVI, WebM, MOV
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