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Comments from British Generic Manufacturers Association and the British Biosimilars Association, and APBI
New approach to cancer therapy pioneered in new lab in Victoria, British Columbia
The need for pharmaceutical serialisation is universally acknowledged but has led to a proliferation of national schemes with no global standardisation; Essentra Packaging looks at why serialisation is only part of the solution to counterfeiting challenges
The implications that are going arise from the UK leaving the European Union are vast and wide ranging
BIA remains committed to making the UK the third global cluster for life sciences
Alwyn Jones, Head of Pharmaceutical and Life Sciences, Siemens UK & Ireland, highlights the company’s new solution for paperless pharmaceutical production that boosts efficiency and makes it easier to introduce personalised cancer therapies, for example
Acquisition of Imugen is expected to contribute approximately $5.5m in revenue during the second half of 2016
Choosing a partner to manufacture potent or highly potent materials requires more consideration than a normal CMO partnership, reports Karolina Narczykiewicz, Operations EHS Manager, Catalent
Project will deliver second cell line to manufacture immuno-oncology antibody ADC-1015 following ADC-1013 success
Regulatory agencies require evidence that disinfection procedures used in pharma cleanrooms are effective and while disinfectants qualified by the vendor, it is also necessary to prove their performance is adequate in a real use scenario. Dr Axel Wehrmann, SGS Life Sciences, outlines the process
Research spotlights increases in funding and recruitment
The handling of ADCs in R&D and manufacturing requires careful examination of the potential health effects that may be caused by occupational exposure. In this first article of a two-part series, John Farris and Robert Sussman, SafeBridge Consultants, discuss the toxicology of ADCs