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Trending Articles
What is ISO 8 cleanroom classification?
Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
CleanLock Module: AES Clean Technology launches new cleanroom airlock
The cleanroom provider has launched its new airlock, which offers a secure transition for people and materials entering and exiting cleanroom environments
New material captures coronavirus particles to boost face mask efficiency
Researchers at the University of Liverpool have looked to significantly boost face mask efficiency by developing a new material that captures coronavirus particles
Cell therapy innovation: Germfree and Orgenesis enter strategic partnership
Germfree and Orgenesis have announced an asset purchase and strategic partnership aimed at advancing Orgenesis’ therapeutic programmes, its suite of product development and...
Impact of the new Annex 1 on sterile filling in pharma
EU GMP Annex 1 is a whole new era for the sterile filling industry. From barrier technology to “first air”, pharmaceutical manufacturers have a lot to decide. Johannes...
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The GMP timeline of adverse event resolution
Regulatory expert Joy McElroy on managing GMP complaints and the steps to resolve incidents ahead of a product recall
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Editor's comment: The devil is in the detail
Common issues that lead to GMP failures are caused by the desensitisation to the value of genuine quality
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Joy McElroy | GMP Consultant
The US-based pharmaceutical manufacturing expert sets the record straight on quality assurance. “Quality is of utmost priority, and top-level management must understand this. We must teach GMPs to them,” she says
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