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Warehouse material handling for pharmaceutical industry

GMPSOP

Raw materials must be inspected to confirm that the containers are intact, have been provided according to the paperwork, and have labels affixed on them identifying the raw material name, batch number, and expiry date. For example, materials with Hold, Quarantine, or Rejected labels must be kept in a quarantine location.

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Six steps process to implement change control management

GMPSOP

Change control management is a systematic process by which a change to facilities, products, systems, or processes is proposed, assessed by a committee (technical and operational impacts), approved, implement, reviewed for effectiveness, and communicated to a larger audience. – Assessment of packaging and labeling components.

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Six steps process to implement change control management

GMPSOP

Change control management is a systematic process by which a change to facilities, products, systems, or processes is proposed, assessed by a committee (technical and operational impacts), approved, implement, reviewed effectiveness, and communicated to a larger audience. – Assessment of packaging and labeling components.

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Sustainable pharma packaging: breaking down the barriers to adoption

European Pharmaceutical Review

For most consumers, product packaging represents their first impression of a brand and its sustainability credentials. But how is this push shaping the pharma packaging market and what are the key changes we can expect to see? For many, aesthetic appeal and user experience top the list of priorities when it comes to packaging design.

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Can holograms help in the frontline fight against pharmaceutical counterfeiting?

European Pharmaceutical Review

One area in which the problem can be tackled effectively is product packaging. With predictions that the global market for anticounterfeiting packaging is set to reach almost $250 billion by 2026, growth in authentication and anti-tamper devices such as holograms appear to have a healthy future.”

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Medication Error Case Examples

RX Note

This incident highlights the potential dangers of unconventional medical abbreviations in prescription communication. I did not identify any errors on medication label and the quantity prepared. Also, similar packaging design across medication strengths can lead to inadvertent selection errors, potentially impacting patient safety.

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How to perform operational qualification – step by step

GMPSOP

– Disintegration Testers (Critical for assessing the disintegration properties of solid dosage forms). – High-Speed Tablet/Capsule Counting Machines (Critical for accurate counting and packaging of tablets and capsules). 90% to 110% of the label claim). What isn't covered in operational qualification?