Biomedical Engineering Reference
In-Depth Information
Attachment Vc
SOP No.: QAS-002
Revision No.:
Issued on:
Initiator sign:
QA In-Process Documents
Check the:
1. Sampling report (manufacturing side)
2. Sampling report (packaging side)
3. QA in-process record of inspection for filling
and packaging of liquids (suspensions, syrups,
drops, etc.)
4. Was there any sorting of product?
5. For each consignee, QA final packaging record
6. Inspection start-up check list for packaging
with release label (packaging area QAI)
7. First signed coded commodities (aluminum
foil, leaflet, box, labels, shipping marks, etc.)
Reasons:
Results:
* In all in-process documents check the presence of hourly checks and confirm that all the physical parameters are within
the specification limits.
Reviewed by:
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