Changes

Ureteral Stent

11 bytes added, 06:18, 2 August 2008
/* Review: Manufacturing documents */
=== Review: Manufacturing documents ===
# Review manufacturing procedures, component specifications, raw material specifications, in-coming and in-process inspection procedures for completeness. # Review linkage between component and raw material specifications and appropriate in-coming inspection procedures. # Ensure inspection procedures have adequate sampling plans based on PFMEA risk mitigation levels – this includes packaging and labeling materials. # Review of calibration records and preventive maintenance records would be also performed. This would also include a review of the in-process / incoming inspection test methods and related test method validations.
=== Validation Report Review ===