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Rapid pseudomonas aeruginosa detection method developed

European Pharmaceutical Review

The study used medications labelled as “sterile, oral and topical preparations, components of formulations for micro-pellicle media, re-agents, and chemical compounds for achieving selectivity, factors promoting multiplication, and inhibition factors.” aeruginosa bacteria in pure culture, mixed culture, or other research materials.

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Supplier qualification standard aims to strengthen supply chains for quality medicines, dietary supplements, and foods

Quality Matters

While focuses on evaluating and establishing supplier reliability for pharmaceutical manufacturing companies and compounding pharmacies, its high-level elements of supplier qualification can also be applied to suppliers of foods and dietary supplement ingredients.

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The Pandemic Treaty and the opportunity to end ‘vaccine apartheid’

pharmaphorum

Tendayi Achium, labelled the response by the global community as a form of “vaccine apartheid,” a suggestion echoed by the organisation’s director general. The UN Special Rapporteur on contemporary forms of racism, E. The discussions over the treaty are set to continue for some time.

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World Standards Day: Recognizing How Standards Enable a Strong Medicines Supply Chain

Quality Matters

In addition to standards for active pharmaceutical ingredients, USP also develops standards for the inactive ingredients (excipients) and other raw materials used in drug manufacturing. In a 2019 report on drug shortages, the FDA found that 62% of drug shortages occur because of quality issues in manufacturing.

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Overview of pharmaceutical quality control steps and implementations

GMPSOP

Certain laboratory reagents are categorized as dangerous commodities, including but not limited to explosives and gases, combustible compounds, peroxides and oxidizing agents, infectious substances and poisons, radioactive materials, and corrosives. Proper labeling and traceability are essential when it comes to reagents.

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Tracking the Drug Trail

Pharmaceutical Technology

” Laser marking solution company Datalase has developed a system where an inactive compound can be added to the tablet formulation. ” LEVEL TRACKING Pharmaceutical manufacturing company Seidenader Vision has also developed a system – the SATrack and Trace.

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What are the elements of quality control process in pharmaceuticals

GMPSOP

Typical flow of samples in a quality control laboratory The quality control laboratory receives samples that are collected randomly at the beginning, middle, and end of manufacturing processes. Quality is everyone’s responsibility, and it should pervade every aspect of pharmaceutical manufacture and packaging.