AUDIT COMPLIANCE REPORT FOR UNAUTHORIZED CORRECTIONS IN BATCH RECORDS
AUDIT COMPLIANCE REPORT FOR UNAUTHORIZED CORRECTIONS IN BATCH RECORDS
1. Context of Observation
During the WHO…
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BMR
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AUDIT COMPLIANCE REPORT FOR FAILURE TO FOLLOW APPROVED BATCH MANUFACTURING RECORD (BMR)
AUDIT COMPLIANCE REPORT FOR FAILURE TO FOLLOW APPROVED BATCH MANUFACTURING RECORD (BMR)
1. Context of…
GxP PRACTICES IN PHARMACEUTICALS
P is a general term used in the pharmaceutical and healthcare industries to refer to various regulatory…
MANAGEMENT OF CLINICAL SUPPLIES IN PHARMACEUTICAL
A clinical trial, in pharma, is like testing a new drug on humans. Volunteers take the drug or a placebo, while…
ANNUAL PRODUCT QUALITY REVIEW
The Annual Product Quality Review (APQR) is a vital process in the pharmaceutical industry, conducted annually…
PRODUCT LIST IN PHARMACEUTICAL
A pharmaceutical product list is a comprehensive catalog detailing the range of medications and healthcare…
BATCH NUMBERING SYSTEM IN PHARMACEUTICAL PRODUCTS
A batch number is a unique identifier assigned to a specific quantity of drug substance or drug product…
MOVEMENT OF BATCH DOCUMENTS IN PHARMACEUTICAL INDUSTRY
These records are created during the manufacturing and packing of a batch to ensure its compliance with quality…
Preparation of Batch Manufacturing and Batch Packing Records.
This SOP has given the procedure for the formation of BMR & BPR in pharmaceutical industry.