Lilly to build new $1bn manufacturing facility in US
The new North Carolinian site will increase parenteral and device manufacturing capacity and create 600 new jobs.
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The new North Carolinian site will increase parenteral and device manufacturing capacity and create 600 new jobs.
This guide explores critical concepts that supply chain professionals need to know about tracking and analysing cold chain pharmaceutical shipments.
How close are we to oral biologic drug delivery? Will biomedical devices be essential in overcoming drug delivery challenges? Discover all this and more in this podcast with MIT's Assistant Professor Giovanni Traverso.
The FDA’s Center for Devices and Radiological Health releases its strategic plan to improve medical device research and regulation for women.
Linda De Jesus, Senior Vice President and Chief Commercial Officer at Azenta Life Sciences highlights the benefits of uniting and focusing efforts solely for the life sciences sector.
Thermo Scientific™ SampleManager™ XR software enables scientists to work hands free to drive process integrity and compliance.
Get the most detailed information about UDI – requirements, implementation and benefits. Everything that supply chain participants need to know!
Find out how to simplify your compliance process and connect data from multiple stakeholders with SAP Advanced Track and Trace for Pharmaceuticals.
This whitepaper considers sterility testing to support pharmacopoeial monographs with an emphasis on products that are difficult to test or validate.
Electronic records and electronic signatures in the regulated environment of the pharmaceutical and medical device industries.
Telstar launches Usifroid global service platform for retrofitting & maintenance of freeze-dryers. To optimise and extend the life cycle of freeze-drying equipment from any brand or model.
This webinar considers the fundamental importance of water system control within pharma processing and the best control and monitoring practices.
Telstar promotes innovative aseptic production solutions in a setting marked by the new GMP Annex 1.
In this webinar, discover how an innovative 2-in-1 method for material analysis accelerates visual and chemical particle analysis in the pharmaceutical industry.
This flyer explains step-by-step how to perform your root cause analysis more efficiently, reliably and cost-effectively with a 2-in-1 solution for visual and chemical particle analysis.