Document control, quality events, and compliance workflows that grow with your pipeline — from research through commercialization. Start in minutes, not months.
You're transitioning from research-grade documentation to GMP, and your current system is a shared Google Drive with 47 folders named "FINAL."
Investors want to see your quality system during due diligence, and you're scrambling to show something that looks professional.
Your team doubled in six months and nobody knows which version of the assay protocol is current.
You need GLP documentation for preclinical studies but GMP readiness for manufacturing scale-up — and your QMS handles neither.
Regulatory consultants keep telling you to "just buy a QMS" but every option requires a six-month implementation you can't afford.
Start lean. Scale as you advance. Never outgrow your QMS.
Start with research-stage SOPs and grow into full GMP documentation as you advance. Version control and approval workflows that scale with your pipeline.
Templates and workflows designed for the messy middle — when you need GLP for studies and GMP for manufacturing, sometimes on the same product.
Version-controlled protocols, method validation documents, and assay SOPs. Stop emailing Word docs between scientists.
Deviations, OOS investigations, and CAPAs configured for lab and manufacturing environments. Root cause tools that scientists actually use.
A professional quality system you can show during due diligence, partner audits, and regulatory interactions. Not a shared drive with "QMS" in the folder name.
Sign up and start working in minutes. Bring your team from zero to functional QMS in days, not months. No consultants required.
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