Batch records on the floor
Digital BMR, IPQC, and release follow the way your line actually runs — materials in, checks at each step, QA out.
Who we build for
A QMS that understands a medical device plant
RapidFacto is written for device manufacturers — not generic life-science software with a medical-device checkbox. Batch records, incoming QC, DHF, and CDSCO paperwork sit in the same system your production team already uses.
Manufacturers using RapidFacto
Trusted by 30+ medical device manufacturers
Quality next to production
Documents, CAPA, training, and complaints are not a separate island. A finding can point at the batch it came from.
India and export in one file
CDSCO, ISO 13485, and Part 11 controls live on the same records. You do not keep a US binder and an India binder.