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Single-use systems have become an important tool in the development and scale up of biotechnology processes. Single-use systems save space, increase flexibility in scale and space planning and, to a large extent, eliminate cleaning costs in development and change over.
12 April 2017 | By Steve Bremer, Managing Editor
The Biophorum Operations Group BPOG has published a best-practices guide for evaluating leachables risk from single-use systems (SUS)...
4 April 2017 | By Christoph Huwe, Strategic Alliance Manager Therapeutics at Bayer Pharmaceuticals, Global External Innovation & Alliances
Ahead of the 7th Annual Strategic Alliance Management for Pharma conference, we spoke with Bayer's Christoph Huwe about the organisational development of alliance management...
31 March 2017 | By Cherwell Laboratories
ImpactAir® high performance air sampler range joins Cherwell’s portfolio of cleanroom microbiology products...
29 March 2017 | By Precision NanoSystems
Precision NanoSystems NanoAssemblr™ platform has been selected for the controlled manufacture of nanomedicines as part of the multinational B-SMART (Brain-Specific, Modular and Active RNA Therapeutics) translational research project...
When processing active pharmaceutical ingredients (API’s), containment is imperative. Not only does this protect the product from contamination, but it also ensures operators are protected from exposure to the highly hazardous materials.
9 March 2017 | By European Pharmaceutical Review
EFPIA, EBE and IFPMA issue joint guidance for prescribers on switching between original reference biologics and biosimilars...
This whitepaper discusses the ISO 14644-1:2015 revisions impacting both the way the cleanrooms are classified and air particle counting instruments...
Commercial biomanufacturing dates to thousands of years and the first biological engine, the yeast, continues to be beneficial...
Near-infrared spectroscopy (NIRS) is a rapid and non-destructive analytical technique that is important in analysing or profiling both solid and liquid dosage forms, as well as biotechnological products...
The use of industrial sieving equipment in pharmaceutical manufacturing is critical to ensure product quality and integrity. To keep up with growing product demand, most pharmaceutical manufacturers must also improve productivity while protecting the health and safety of operators.
Read the free-to-view digital version of the latest issue of European Pharmaceutical Review...
22 February 2017 | By Professor Josep Tabernero, Chair of the ESMO Cancer Medicines Working Group
Dr Josep Tabernero explains the benefits of biosimilars, showing how they can create sustainable, safe and affordable access to medicine globally...
The first part of an in-depth article on Quality by Design (QbD), published in European Pharmaceutical Review in December 2016, focused on designing quality in to a pharmaceutical drug product by considering dosage form design, and understanding the importance of active pharmaceutical ingredients’ (APIs’) and excipients’ properties.
21 February 2017 | By GE Analytical Instruments
This webinar demonstrated Total Organic Carbon (TOC) feasibility, method validation and transfer from the laboratory to the manufacturing floor, as well as reviewing a feasibility study for multiple, difficult to oxidise or low solubility organic compounds...
