mislabelling – Pharma GMP

Case Studies: Packaging Errors That Led to Recalls

digi — Tue, 25 Nov 2025 17:27:04 +0000

Case Studies: Packaging Errors That Led to Recalls Step-by-Step Tutorial on Avoiding Packaging Errors in Pharmaceutical Manufacturing Packaging line controls in pharmaceutical manufacturing represent a critical control point to ensure patient safety, product integrity, and regulatory compliance. Errors such as mislabelled packs, application of the wrong leaflet, and mix-ups on the packaging line have repeatedly...

Audit Findings on Mismanaged Printed Packaging Material Storage

digi — Tue, 25 Nov 2025 08:48:04 +0000

Audit Findings on Mismanaged Printed Packaging Material Storage Comprehensive Step-by-Step Guide to GMP Storage of Printed Packaging Materials: Preventing Audit Findings and Ensuring Compliance The pharmaceutical industry demands stringent control over every aspect of drug product manufacturing, including raw materials, components, and packaging materials. One commonly encountered area of regulatory scrutiny involves the gmp storage...

How to Handle and Record Discrepancies During Raw Material Receipt

digi — Tue, 25 Nov 2025 05:12:04 +0000

How to Handle and Record Discrepancies During Raw Material Receipt Step-by-Step Guide: Handling and Recording Discrepancies During Raw Material Receipt The raw material receipt and quarantine procedure is a critical component of pharmaceutical Good Manufacturing Practice (GMP), ensuring that inputs into the manufacturing process meet quality and regulatory standards. A robust procedure is necessary to...