What if you could write any URS in 15 minutes?

Document automation for biologics and vaccines manufacturing

Transform your approved Word templates into guided forms. Generate consistent, audit-ready GMP documents in minutes.

Be first to know when we launch. No spam, ever.

✓ You're on the list! We'll be in touch soon.
Stainless steel bioreactors in a GMP biopharma manufacturing facility

See how it works

Fill a guided form, generate a complete document

EnjiPro guided form for TFF User Requirements Specification with dropdowns for operating mode, process steps, and product type

Guided form with smart dropdowns

→
Generated Word document showing TFF URS with requirements table

Generated Word document

Why engineers love EnjiPro

Never start from scratch

Stop copying from old documents and fixing outdated content. Start with a guided form pre-loaded with the right options.

No more formatting headaches

Tables, headers, numbering — all handled automatically. Your output matches the approved template every time.

No risk of missing requirements

Guided forms ensure every parameter is considered. No more forgotten specifications or incomplete sections.

Use our library or your own templates

EnjiPro works with standard biopharma document structures. Start with our pre-built templates or import your company's approved formats.

Template library

Ready-to-use templates for URS, equipment specs, qualification protocols, and more

Import your own

Upload your company's Word templates and we'll convert them to guided forms

Bioreactor URS TFF System URS Chromatography Skid URS CIP System URS Equipment Specifications Buffer Lists Media Lists Raw Material Lists Consumables Lists IQ Protocols OQ Protocols PQ Protocols Tech Transfer Plans Process Descriptions

Document types we support

Covering the full spectrum of biopharma manufacturing documentation

User Requirements Specifications (URS) Equipment Specifications Tech Transfer Plans Buffer Lists Media Lists Raw Material Lists Consumables Lists Qualification Protocols Validation Documents IQ/OQ/PQ Protocols Process Descriptions Batch Records
GMP Certified badge

Built for GMP compliance

EnjiPro is designed with pharmaceutical manufacturing requirements in mind. Ensure traceability, consistency, and regulatory compliance across all your documentation.

Hamid Trimech, Founder of EnjiPro

Hamid Trimech

Founder — Biopharmaceutical Engineer & CMC Consultant

10+ years in vaccine and biologic manufacturing. 15+ vaccine programs across 13 countries. 4 GMP facility constructions led. Contributed to two approved COVID-19 vaccines. After years of writing URS, equipment specs, and validation documents by hand, I built EnjiPro to give engineering teams their time back.

15+ vaccine programs 13 countries 4 GMP facilities built 2 books published
VaxEng Biomanufacturing Made Simple LinkedIn

Ready to transform your document workflow?

Join the waitlist and be among the first to experience EnjiPro.

✓ You're on the list! We'll be in touch soon.