Whitepaper: The necessity of E&L qualifications for lyophilised drug products
Lyophilised drug product containers and administration devices consist of the primary packaging, the reconstitution solution container, and the drug administration set.
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Lyophilised drug product containers and administration devices consist of the primary packaging, the reconstitution solution container, and the drug administration set.
G-CON cleanroom PODs. Reliable, flexible prefabricated cleanrooms for the biopharmaceutical industry. On budget and on time.
In this 10-minute tutorial you will learn how to overcome the main challenges when selecting a medium for media fill tests or aseptic process simulations.
Enjoy ingenious products and packaging solutions with individual support to keep you safe, simplify your lab work, and help you save resources.
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13 January 2021 | By Altasciences
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The EMA has received a conditional marketing authorisation application for the Oxford-AstraZeneca COVID-19 vaccine.
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Rising at a CAGR of 8.2 percent, the rapid microbiology testing market is predicted to grow over the next five years.
A summary of the current state of container closure integrity testing in the pharmaceutical industry.
This on-demand webinar focuses on the importance of cleaning and disinfection, covering legal requirements and the global guidelines for disinfection in cleanrooms.
Researchers have shown that microbial surface recovery using contact plates was superior on vinyl than stainless steel.