Document control, CAPAs, supplier management, and audit readiness — for teams who'd rather build products than negotiate software contracts.
Every approval adds a ring.
Every controlled document, every approval, every signature in one living record.
Sign up, pick a template from the ISO 13485 pack, ship your first SOP.
Hosted on Azure with point-in-time recovery and full audit export.
Built by medical device engineers who got tired of QMS tools that require a sales call to open.
Versioning, approval workflows, periodic review, and side-by-side diff. Every change carries its rationale.
CAPAs, NCRs, and complaints with configurable templates that map cleanly to your process.
Onboarding, qualification, and re-evaluation workflows out of the box. Re-qual reminders never miss.
Pre-built starter templates — quality manual, SOPs, work instructions, forms. Branch and edit from day one.
Full history of who changed what and when. Always exportable. Always notarized. Always audit-ready.
Sign up, swipe a card, start working. The "demo required" gate is what we're here to remove.
Legacy QMS tools gate everything behind demos, procurement, and enterprise reps. By the time you have a login, you've lost weeks you could've spent building your product. We built ArvoDocs so you can sign up and start working — today.
Start free. Upgrade when your process matures. Always month-to-month.
For early-stage teams getting their first SOPs under control.
For growing teams that need the full toolkit.
For established teams with advanced compliance needs.
Peer support, not ticket queues. Connect with other medical device teams, share templates, and trade audit war-stories.
Join us on Slack →