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Guide To Testing
In this edition of our ‘Guide to’ series, learn how these leading companies’ services and expertise can help you test your pharma/ biopharma products and medical devices.
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Cleanrooms
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Aseptic containment strategies to meet challenges of processing new highly toxic and biologically hazardous sterile medicinal products and therapies
Active pharmaceutical ingredients (APIs) have been established in the pharmaceutical industry over the course of many years. Containment technologies – ie, those strategies developed to contain the APIs – and qualification practices based on API powder containment have primarily been based on health and safety issues related to operator exposure…
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Microbiological considerations in cleanroom validation
Wickham Laboratories Ltd is delighted to announce our most recent technical article on, “microbiological considerations in cleanroom validation”, which has been featured in European Pharmaceutical Review’s December 2018 issue...
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Application Note: Microbiological considerations in cleanroom validation
Contamination, microbiological or otherwise, is a key safety concern in the development and manufacture of all pharmaceuticals and medical devices.
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One stop to meet contamination monitoring regulations
Presenting solutions that Particle Measuring Systems provide in total concept including training, services and their FMS system which monitors instruments.
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Wickham Laboratories Ltd to exhibit at Pharmig 2018
Wickham Laboratories will be exhibiting at Pharmig’s 26th annual conference held on the 28 and 29 November at the Belfry Hotel, Nottingham...
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Wickham Laboratories: Drawing on deep technical expertise
Wickham Laboratories draws on deep technical expertise, backed by decades of global experience, when identifying challenges and providing solutions for a broad range of products and testing scenarios.
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Perceptive Engineering: Spotlight on… Continuous Manufacturing
In this Spotlight on Continuous Manufacturing, Perceptive Engineering creates industrially robust solutions using advanced model-based control and monitoring technologies...
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G-CON: Spotlight on… Continuous Manufacturing
In this Spotlight on Continuous Manufacturing, G-Con explains how they have simplified the entire design/build/validate process via their prefabricated cleanroom infrastructure line...
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CPD-certified conference programme for Lab Innovations 2018
Two days of free science focused presentations...
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How the new draft of Annex 1, Manufacture of Sterile Medicinal Products impacts environmental monitoring programmes
This article explores how the new draft of Annex 1, Manufacture of Sterile Medicinal Products impacts environmental monitoring programmes.
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NewAge® Industries/AdvantaPure® completes plant expansion for additional clean room manufacturing suites
Following nearly two years of planning, preparation, construction and validation, team members at NewAge Industries/AdvantaPure are now using new clean rooms to produce platinum-cured silicone tubing, molded components and Single-Use molded tubing assemblies...
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AdvantaPure® introduces new case studies on tubing, closures and molded assemblies
AdvantaPure has released three new case studies focused on fluid transfer challenges involving biopharm and pharmaceutical applications. Each Study Describes Processing Problems, Customer Goals, and Product Solutions...
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Scientific Poster: From Screening to Small Scale GMP Biomanufacturing: Exploring a simple, unified platform strategy for handling a range of cell culture needs
This poster discusses a process for a 12-week clone development process. The process starts in silico, and progresses through screening and clone selection in 96-deepwell plates up to five liter shaker flasks...
