Create
Generate standardized drafts from approved templates.
Products
Everything You Need to Create and Control Compliance Documentation
SCRPTA brings document generation and controlled document management together so regulated manufacturers can standardize creation, govern approvals, and stay audit ready.
- 1Create
- 2Review
- 3Approve
- 4Release
- 5Revise
- 6Audit
Secure communication
Business inquiries handled through protected channels.
Manufacturing expertise
Built for regulated medical device documentation workflows.
Personalized demos
See the platform mapped to your documentation process.
One Platform. Two Focused Products.
SCRPTA is a Compliance Documentation Platform — not an eQMS, PLM, or ERP. It focuses on the documentation workflows manufacturers rely on every day.
Platform Architecture
Review
Collaborate across engineering, quality, and regulatory teams.
Approve
Route documents through controlled approval workflows.
Release
Publish current controlled documents for operational use.
Revise
Manage updates without losing history or clarity.
Audit
Retrieve evidence quickly when inspections happen.
Product Overview
Explore the two products that make up the SCRPTA Compliance Documentation Platform.
Product
Compliance Document Generation
Create standardized compliance documents using reusable templates, controlled formatting, and consistent structures.
- Template-based authoring
- Reusable content blocks
- Document numbering
- Draft management
Product
Controlled Document Management
Maintain complete control over versioning, approvals, access, revisions, and audit-ready document history.
- Version control
- Approval workflows
- Access control
- Audit-ready history
Feature Comparison
See how the products complement each other across the documentation lifecycle.
| Capability | Document Generation | Document Management |
|---|---|---|
| Template-based document creation | ||
| Reusable content blocks | ||
| Version control | ||
| Approval workflows | ||
| Access control | ||
| Audit trail and history | ||
| End-to-end documentation lifecycle |
Frequently Asked Questions
Many manufacturers benefit from both. Document Generation improves how documents are created, while Controlled Document Management governs how they are reviewed, released, and maintained.
No. SCRPTA is a Compliance Documentation Platform focused on document generation and controlled document management for regulated manufacturers.
Yes. Documents can be generated with standardized structures and then managed through controlled review, approval, release, and revision workflows.
Quality, regulatory, engineering, manufacturing, and documentation teams in medical device and other regulated manufacturing environments.
Ready to Modernize Your Documentation Process?
Request a demo to see how SCRPTA supports compliance document generation and controlled document management.