Batch dossier in one place
Materials, manufacturing, IPQC, FG testing, wastage, and release — the tabs they flip through, already filled.
India MDR 2017
The inspector should not wait while you find the file
CDSCO walks the floor. They ask for the BMR, the incoming inspection, the training record, and the last CAPA. RapidFacto keeps those on the batch and the product — not in a cupboard labelled “audit”.
Manufacturers using RapidFacto
Trusted by 30+ medical device manufacturers
Who signed, and when
Role-based approvals and e-signatures. Shared logins do not survive this conversation.
Trace a lot either way
Which batches used this incoming lot? Which lots went into this batch? That answer is a filter, not a weekend.