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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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White background with conference logos (GCSG, CTS East Coast, and OCT & CTS Nordics)

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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What's the average time to bring a drug to market in 2022?

COVID vaccines and antivirals sped through clinical trials and regulatory approvals in record time. But these records are even more impressive when you...

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