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Study reveals the risk inactive ingredients pose
Researchers have found that many pharmaceutical products contain inactive ingredients which can be dangerous to patients.
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Ingredients
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Pharmaceutical intermediates market to see growth
The global pharmaceutical intermediates market is likely to see year-on-year growth in 2019, by an estimated 3.6 percent rate.
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Nelson Labs: supporting internal quality processes
Nelson Labs has a long history of partnering with pharmaceutical and biopharmaceutical companies. We perform a variety of testing to support your internal quality processes including: sterility (USP 71) testing in a cleanroom for isolator environment, particulates testing (USP 787, 788) using a variety of methods, bacterial endotoxin, filter validations,…
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Eurofins BioPharma Product Testing
From starting materials through to finished product testing, Eurofins BioPharma Product Testing’s 34 facilities in 17 countries deliver a comprehensive scope of harmonised GMP testing services and seamless regulatory acceptance.
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Strong line-up for Chemspec Europe 2019
Chemspec Europe 2019 gathers impressive array of industry experts under one roof
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Expert View: Advancing bacterial endotoxin testing with recombinant Factor C
Emerging recombinant Factor C (rFC) methods have many advantages to offer pharmaceutical quality control, including improved specificity, robustness, efficiency and alignment with 3R principles. First, global manufacturers have validated rFC and pharmacopoeias worldwide are on the move. Here, Karolina Heed provides an industry and regulatory update.
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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.
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Whitepaper: The performance of PROSOLV® EASYtab SP in four medium-dose
In the present study, the performance of PROSOLV® EASYtab SP was tested in four DC formulations with different model APIs. Each of the selected APIs presented a particular challenge in terms of producing tablets with suitable hardness, weight, uniformity, content uniformity and/or reliable dissolution profiles.
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Setting the standard for water quality measurement and control
A brief overview of how SWAN Analytical Instruments helps to ensure water quality with analysers to measure trace ozone and total organic carbon (TOC).
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No-deal Brexit ‘catastrophic’ for science and innovation in the UK
Seventy-two percent of chemistry professionals said that a no-deal Brexit would be “very negative” for the sector, survey finds...
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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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Flyer: Sterile manufacturing – finished dosage forms
Eurofins CDMO provides a wide range of aseptic processing services for all drug product configurations with flexibility to accommodate a wide range of compounds, primary packaging systems, batch sizes and fill volumes to help develop your Active Pharmaceutical Ingredient or bulk product into Finished Dosage Forms for use in clinical…
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Drug delivery to the heart with tannin acid may avoid surgery
Tannin acid injections to treat cardiovascular disease may avoid the need for surgery, according to research from Korea...
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‘Nano-submarines’ to help target headaches and tumours
Tiny drug-filled nanocarriers, termed ‘nano-submarines’, are being developed to boost the targeted treatment of headaches and tumours, without damaging healthy tissue...
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Metabocin shows promise as a potent anti-obesity treatment
A novel drug based on capsaicin caused long-term weight loss and improved metabolic health in mice eating a high-fat diet...
