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Transform pharma training videos into FDA-compliant, auditable documentation. Perfect for pharmaceutical manufacturers, biotech companies, and CROs managing GMP training and regulatory compliance.
Watch It Work
See how pharma training videos become FDA-compliant documentation instantly
Join pharmaceutical companies using Docsie to convert training videos into auditable compliance documentation
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GMP training videos become FDA-compliant, auditable documentation
Why Docsie is Different
Most tools just convert speech to text. Docsie's multimodal AI actually watches your videos—reading on-screen text, identifying UI elements, and understanding visual context.
AI watches and understands video content—reads on-screen text, identifies UI elements, detects visual changes, and understands what's happening in each frame
Correlates what's being said with what's being shown. Understands technical terminology, product names, and industry jargon—no more 'sequel' instead of 'SQL'
Identifies important visual moments—UI changes, diagram reveals, key screens—and captures them as illustrations correlated with text
Simple Process
Powered by Docsie Copilot's agentic AI system
Drop your training video, product demo, or tutorial into Docsie. Supports all major formats: MP4, MOV, AVI, WebM
Multimodal AI watches the video, reads on-screen text, identifies UI elements, and creates structured documentation in real-time
Get professionally formatted documentation with screenshots, step-by-step instructions, and structured content ready to publish
Everything you need to convert pharma training videos into FDA-compliant documentation
Generate documentation with timestamps, version control, and audit trails that support FDA regulatory requirements
Automatically identify and structure Good Manufacturing Practice procedures, critical process parameters, and quality control points
Convert training videos into documentation in multiple languages for global manufacturing sites and regulatory submissions
Generate searchable documentation with automatic linking to FDA regulations, ICH guidelines, and internal SOPs
Automatically capture critical visual evidence of equipment setup, manufacturing processes, and quality checks
Structure documentation to support IQ/OQ/PQ validation with step-by-step procedures and acceptance criteria
Watch how Docsie Copilot analyzes both audio and video—seeing UI elements, reading on-screen text, and capturing code—to create structured documentation
No credit card required • 14-day free trial
Common Questions
Everything you need to know about converting pharma training to FDA-compliant documentation
Q: Can I use this for FDA-regulated documentation and GMP training?
A: Yes. Docsie generates documentation with audit trails, version control, and timestamps that support FDA regulatory requirements. The system maintains a complete record of all changes and helps create documented evidence of training completion for regulatory submissions.
Q: Can I use this for GMP training documentation required by FDA?
A: Absolutely. Docsie converts GMP training videos into written procedures, SOPs, and training records that FDA auditors expect to see. The system automatically structures content to match GMP documentation requirements and maintains traceability to the original training video.
Q: How does this handle validation protocols (IQ/OQ/PQ)?
A: Docsie's AI recognizes validation terminology and automatically structures Installation Qualification, Operational Qualification, and Performance Qualification procedures. It captures acceptance criteria, test procedures, and results documentation in a format suitable for validation packages.
Q: Does the AI understand pharmaceutical terminology and GMP concepts?
A: Yes. Our multimodal AI is trained on pharmaceutical and regulatory content. It recognizes GMP terminology, regulatory citations (21 CFR, ICH guidelines), process validation concepts, and pharmaceutical manufacturing procedures—ensuring accurate documentation that doesn't misinterpret critical compliance terms.
Q: Can I customize the documentation format for our QMS?
A: Yes. The AI-generated documentation serves as a structured first draft that you can edit and format to match your Quality Management System requirements. All SOP numbering, formatting, and approval workflows can be customized while maintaining the core content integrity.
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
Start creating professional documentation that your users will love
