Nonconformance (NCMR) Investigation and MRB Disposition demo
The material review board sits at a table set with the records: every option weighed for and against, use as is held at a gate, and every seat signing for itself. 1:27
What the demo shows
An NCMR and MRB disposition solution for device plants: evidence pulled, every seat signs.
When a lot is held, agents pull the traveler, supplier certificate, CMM report and program history, furnace chart and calibration log, weigh each possible cause for and against, and draft a disposition with its code. For every option they show what would make it wrong; use as is and repair stop at a gate until design engineering gives a rationale and the risk file check passes. Each seat opens its records and signs for itself, and a systemic cause opens a CAPA with the packet.
Transcript
- NCMR Investigation and MRB Disposition prepares device plants' material review boards.
- FDA cited nonconforming product control 95 times in fiscal year 2025, by one industry count.
- Nine of 13 sampled shells read thin; all 140 are held.
- They trace it to a program change measuring from the coated pole.
- The draft is a sort; Pritha signs as author, in her own session.
- Leontine switches to her own view, opens the drawing and the risk file herself, and rejects use as is.
- Tobiah signs in as himself, opens the program check, and agrees for manufacturing.
- Re-measured on rev E, 96 pass; 44 are scrapped, three kept as evidence.
- Every signature and its session lands on the audit trail.
- The result: 96 shells kept for an independent check, 44 scrapped.
- Built on Botminds: agents, data, screens and governance on one platform.
The narration as written for the film. Captions are on the player.