ADDITIONAL PAGE ISSUANCE OF CONTROLLED DOCUMENTS

Description

In the pharmaceutical industry, controlled documents are crucial for maintaining quality and compliance. These documents, such as Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and Batch Packaging Records (BPRs), need to be updated and revised regularly to reflect changes in processes or regulations. When a controlled document requires an additional page, a specific procedure must be followed to ensure proper control and traceability.