Company
Built next to the line, not from a generic QMS playbook
RapidFacto started with plants that were still filling BMRs by hand and keeping SOPs on a shared drive. We write software for that work — medical device manufacturing in India, and the inspections that come with it.
Manufacturers using RapidFacto
Trusted by 30+ medical device manufacturers
What we do
Document control, CAPA, training, design, purchase, and batch records in one system. The report you print for CDSCO or an ISO auditor is the same data operators entered on the floor.
Why devices
Device plants have a specific problem: lot traceability, incoming QC, DHF, and a shop-floor BMR that has to match. We stay in that problem. We do not sell a life-science suite and hope manufacturing fits.
How we work
Implementation is scoped to your products and SOPs. You keep the data. You can export records and reports. We validate the software and give you the package your QA team will ask for.