All eyes are on those on the front lines seeking to develop and produce new drugs. There’s unprecedented pressure to offer both immediate treatments for those affected and long-term biotherapies and vaccines to prevent future epidemics.
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Keys to accelerating your COVID-19 drug campaign
As SARS-CoV-2 moves fast through our global population, the pharmaceutical industry faces tremendous pressure to move even faster.
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How to deliver multi-product ATMP facilities for future flexibility
Manufacturers must produce a variety of ATMPs quickly and efficiently. Enter the multi-product ATMP facility.
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Reducing waste with lean delivery in facility design and construction
Applying a lean delivery approach to the design and construction of new facilities can reduce waste, lower costs and improve speed to market.
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NextGen Now: Delivering tomorrow’s facilities today
If cell and gene therapy products are to successfully reach patients and deliver transformative cures, then the industry will need more facilities capable of manufacturing them.
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Advanced therapy medicinal product facilities through the eyes of a process architect
Advanced therapy medicinal product (ATMP) companies are ushering in a new frontier of medicine and technologies poised to revolutionize human health, but are ATMP facilities keeping up? The industry is advancing at such a rapid pace that these companies are faced with vast new complexities when developing and manufacturing their products.
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How biopharma facilities can use ice in a glycol chiller system
Ice storage, coupled with a glycol chiller, can provide benefits that other options can’t.
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When to close your pharmaceutical process
Too often, the term “closed process” is thrown around without an understanding of the salient issues. Pharmaceutical process closure can certainly provide many benefits, but there are various impacts and requirements depending on the ultimate goal and the specific process you are trying to close.
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How to choose a contract manufacturing organization
The age-old debate of whether to outsource production to a contract manufacturing organization (CMO) remains for mature, emerging and virtual biopharmaceutical companies.
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Improving documentation change control process
In regulated environments, companies are expected to establish procedures for document change control as a way of ensuring product quality and safety.
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