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IRT optimization in clinical trials: achieving maximum efficiency
Clinical trial supply managers work hard to ensure trial protocols, supply plans, and resupply strategies are designed for maximum efficiency.
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Curb drug waste and improve your clinical trial strategy
An average of 95% of clinical supply managers face some level of supply risk during their trials. Moreover, supply chain bottlenecks can generate 2 to 4 months...
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Let's meet at our next conferences!
After a couple of quieter summer months, N-SIDE is headed to conferences again! Missed us last year or want to meet with us again? You're in luck! Find out which...
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5 key considerations for clinical trial packaging and labeling
Designing the packaging and labeling for investigational new drugs (INDs) and investigational medicinal products (IMPs) can be a complex task — especially when...
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The 3 biggest challenges in the clinical trial supply chain
Drug supply chain management is a balancing act. You need to ensure enough drug is available to meet patient demand and that supply is allocated where it’s most...
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How to optimize your clinical trial manufacturing plan
Are you making the best possible decisions about your clinical trial manufacturing?
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Meet our team at the BSMA Conference in Foster City, CA
Join us at the BSMA Conference in Foster City in June! The N-SIDE team will be attending the BSMA Conference in Foster City, on June 22-23. Come by our booth and...
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What is clinical supply chain software?
As clinical trials become more complex and expensive, it becomes even more important that they go smoothly from the start. Thankfully, clinical supply chain...
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N-SIDE announces new partnership with BeiGene
N-SIDE, a deeptech company that empowers life sciences organizations to make better decisions and optimize the use of critical resources, is pleased to announce...
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