iPDF: Environmental monitoring solutions for pharmaceutical industry
Our environmental monitoring solutions for cleanrooms and isolators cover microbial air, compressed gas, surface and personnel monitoring solutions.
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Our environmental monitoring solutions for cleanrooms and isolators cover microbial air, compressed gas, surface and personnel monitoring solutions.
This issue includes articles on Raman mapping of pharmaceutical tablets, delivery options for mRNA therapeutics, the use of high-throughput analytics for clonal cell selection and much more...
This extensive resource guide for LC-MS brings our complete portfolio of columns, consumables and accessories developed to ensure reliable analysis.
What is driving the adoption of rFC for BET? Alternative methods are the obvious sustainable solution for efficient manufacturing.
A guide through the maze of chiral HPLC columns for versatile and robust Chiral HPLC and LC-MS separations.
Protocol for purification, proteolysis, reduction and UHPLC-MS analysis of unlabelled and labelled monoclonal antibodies
Available on-demand: experts discussion and Q&A on the recent annex 1 revision, in the context of Microbiological Environmental Monitoring.
Webinar now on-demand: Analysis of nitrosamines in drugs using chromatographic methods according to regulatory requirements.
A new regulatory group, part of the European Medicines Agency, will aid innovative approaches for the development and quality control of medicines, including new technologies for EU patients.
Researchers demonstrate ultra high performance liquid chromatography with triple quadrupole mass spectrometry to detect and quantify trace amounts of cephapirin and ceftiofur.
Use this filtration selection guide as a starting point for selecting and sizing the most appropriate Millipore® filter.
Monkeypox oligos - Primers & Probes for Research & Commercial use.
Over the last 10 years, there has been an important change of focus in pharma towards biotech products and personalised therapies. These important new treatments are now emerging into manufacturing, with implications for the way that quality is monitored, managed and assured. Dr Eduard Cayón sets out some practical advice.
The International Society of Pharmaceutical Engineering’s GAMP® 5 guidelines steer validation practices for pharma companies to meet computerized system expectations. Members of the GAMP steering committees, Lorrie Schuessler, Charlie Wakeham and Stephen Ferrell, share the some of the key changes in the second edition update and how these should be…
Merck and Novatek International team up to monitor contamination and enhance environmental monitoring in the pharmaceutical industry.