news
Patent litigation for adalimumab resolved in the US
AbbVie has announced that it has resolved its US HUMIRA (adalimumab) litigation with Boehringer Ingelheim.
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Manufacturing
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Steriline products and solutions: Intelligent compounding systems
As a single-source supplier of equipment solutions for the primary packaging of injectable drugs, Steriline develops, manufactures and supplies a comprehensive range of solutions, including both mechanical and robotic applications for the aseptic processing.
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Steriline products and solutions: Robotic applications
As a single-source supplier of equipment solutions for the primary packaging of injectable drugs, Steriline develops, manufactures and supplies a comprehensive range of solutions, including both mechanical and robotic applications for the aseptic processing.
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Steriline products and solutions: Isolators
As a single-source supplier of equipment solutions for the primary packaging of injectable drugs, Steriline develops, manufactures and supplies a comprehensive range of solutions, including both mechanical and robotic applications for the aseptic processing.
news
Faulty barcode scans could cost the pharma industry billions
Pharmaceutical manufacturers and wholesale distributors could start losing billions of dollars because of faulty barcode scans.
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Nemera at Interphex 2019
Nemera is a world leader in the design, development and manufacturing of drug delivery devices for the pharmaceutical, biotechnology and generics industries.
webinar
The role of an integrated LIMS solution on supporting data integrity in current cGMP environments
14 May 2019 | By Abbott Informatics
Understand the role of data integrity in current good manufacturing practice for drugs as required in 21 CFR parts 210, 211, and 212.
news
New guidance issued for 3D-printed Medical Device License applicants
Health Canada has published new guidance for manufacturers of higher-risk 3D-printed medical devices.
article
It’s not just about the science: microbiological analysis
Modernisation of microbiological test methods involves far more than just the science. As new systems and technologies become available it becomes increasingly important that potential users can identify not only the technical requirements, but also the business case. Here, Paul Newby, Alice Laures and Lisa Wysocki from GlaxoSmithKline discuss criteria…
whitepaper
Case Study: Using AdvantaSil™ High Pressure Unreinforced Silicone Tubing for bulk fluid transfer
The transfer of bulk liquids, such as media, buffer and intermediates, are critically important in biopharmaceutical production processes. This case study describes the performance of AdvantaSil High Pressure Unreinforced Silicone Tubing (APHP) used in a Monoclonal Antibody process for the transfer of buffers in purification.
news
Taking the difficulty out of API process filtration
Amazon Filters has selected the Making Pharmaceuticals Exhibition & Conference 2019 to showcase its latest filter housings and microfiltration filter cartridges, which are used in the manufacture of Active Pharmaceutical Ingredients (API) and are the essential components when creating pharmaceutical products.
video
Sepha VisionScan: Non-destructive, deterministic blister leak testing down to 7µm
Introducing a smart alternative to traditional blue dye test methods. The Sepha VisionScan uses a non-destructive method to provide reliable, objective and deterministic results. The machine doesn’t require tooling, making it ideal for production lines running multiple products.
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European Pharmaceutical Review Issue 2 2019
This issue questions whether companies are sufficiently investing in regulatory intelligence software and what the potential consequences of Brexit might be for locations outside of the UK and EU. The issue also features articles on microbiology, formulation and biopharma, courtesy of our in-depth focus sections; as well as outlining the…
whitepaper
Application note: Cleaning validation from HPLC to TOC: three factors to consider
This application note from SUEZ outlines the factors that companies should consider when choosing their cleaning validation procedure, highlighting the benefits of TOC analysis over HPLC.
whitepaper
Flyer: API commercialisation
Eurofins CDMO works closely with clients to provide phase-appropriate solutions to balance any immediate and long-term API technology development and commercialisation needs.
