About RapidFacto

Our Mission

RapidFacto exists to simplify compliance and quality management for medical device manufacturers. We believe that maintaining ISO 13485 and CDSCO compliance shouldn't require mountains of paperwork and manual processes.

Our software automates documentation, streamlines workflows, and ensures every manufacturing step is audit-ready — saving manufacturers up to 90% of their documentation time.

Our Story

Born from years of experience working directly with medical device manufacturers in India, RapidFacto was built to solve the real pain points we saw every day: lost documents, failed audits, manual batch records, and compliance headaches.

We started by digitizing Batch Manufacturing Records and quickly expanded to cover the entire quality management lifecycle — from document control and CAPA to training management and internal audits.

Why Medical Devices?

The medical device industry has some of the strictest regulatory requirements. CDSCO inspections, ISO 13485 audits, and GMP compliance demand meticulous documentation at every step. We specialize in this domain because we understand these unique challenges and build solutions specifically for them.

What Sets Us Apart

• Domain expertise — built by people who understand medical device manufacturing regulations
• Complete audit trail — every action is logged and traceable
• One-click reporting — generate BMRs, CoAs, and inspection reports instantly
• Cloud-based — access your QMS from anywhere, on any device
• Easy to use — designed for manufacturing teams, not IT departments