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FDA encourages appropriate prescribing of opioids
The FDA has updated its Opioid Analgesic REMS to ensure caregivers and patients use opioids effectively...
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Manufacturing
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SPC manufacturing waiver is good news for Europe
An SPC manufacturing waiver should be extremely beneficial for Europe and will increase net sales of the EU pharmaceutical industry...
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Radiance could be the key to faster viral detection
Viruses explored through Radiance, an instrument designed to improve the process of analysis, ensures quick and efficient viral detection...
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Driving real-time productivity insights with connected laboratory automation
Tecan is offering its customers unprecedented insight into how their Fluent® and Freedom EVO® liquid handing platforms are being used, thanks to its Introspect™ and Common Notification System (Tecan CNS™) software tools...
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Quality Assurance / Pharmaceutical Quality Systems in manufacturing medicinal products
Quality Assurance (QA) covers all aspects that could have an impact on the quality of prescribed pharmaceutical products. This article focuses on some of the Pharmaceutical Quality Systems in relation to QA of manufactured medicines.
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Spotlight on… Manufacturing
In this Spotlight on Manufacturing, ACG explains how it meets clients’ changing needs and identifies emerging market trends...
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Spotlight on… Single use
In this Spotlight on Single Use, David Beattie, Vice President BioProcessing R&D, Merck explains the mode of operation and benefits of its Pellicon® Capsules...
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HD vein imaging aids intravenous injections
Near-infrared light can now be used to aid clinicians in identifying veins in patients, especially when this process becomes difficult...
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Peak Scientific has launched its first high-flow hydrogen carrier gas generator. See it first at JASIS 2018!
Peak Scientific, the global leader in gas generation for analytical laboratories, has introduced a new hydrogen gas solution to the market, the Precision Hydrogen Trace 1200...
whitepaper
Application Note: Gas safety in the laboratory
Modern laboratories use a number of gases as part of their daily operations. This application note details two of the most common methods of laboratory gas supply, and their associated safety risks and benefits...
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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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SciLabware introduces sterile ready-to-use WHEATON® COMPLETEPAK
WHEATON® COMPLETEPAK is a range sterile, ready-to-use and off the shelf primary packaging components, which can be customised for any application...
whitepaper
Whitepaper: Why should you care about Burkholderia cepacia?
The Burkholderia cepacia complex (BCC) species are a group of gram-negative, rod-shaped bacteria that have been shown in recent years to be of concern for patients, and thus for manufacturers of drugs and products that contribute to patient health...
webinar
Understanding current CFR 21.11 and data integrity requirements
8 August 2018 | By SUEZ
The US FDA and European Commission have defined regulations relating to the submission of electronic records in lieu of paper documents, for submission, inspection, and archiving purposes. When ageing analytical equipment is to be replaced 21CFR Part 11 and EU Annex 11 are also topics of discussion. Common questions from…
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Boosting the safety of bulk drug substances is aim of FDA measures
Boosting the safety of compounded drugs is the aim of new plan from the US Food and Drug Administration (FDA), which has unveiled a series of measures.
