Biomedical Engineering Reference
In-Depth Information
Attachment Vg
SOP No.: QAS-002
Revision No.:
Issued on:
Initiator sign:
Packaging Area Documents
Check the:
1. Batch packaging record for the presence of
all the entries and correctness of the
manufacturing and expiry date as per shelf-life
2. Batch packaging record for
a.
Hand packing line (if applicable)
b.
Suppositories filling and packing
3. Packaging report and release of finished
product (for different consignee)
4. Packaging materials requisition
5. Batch yield final and at various in-process
stage is correct
6. Rejection verification at various stages of
processing and at final stage
7. Reconciliation of labels and boxes done by
the packaging department
8. Area/equipment line clearance for
packaging operation
9. MPI for different consignee
10. Output sheet
11. Repacking addendum
12. Store requisition for the repacking material
Remarks:
Reviewed by:
Page 3 of 5
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