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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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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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International Day of Women and Girls in Science: N-SIDE celebrates the daily commitment of its female colleagues!
On this International Day of Women and Girls in Science, we are especially proud to celebrate the daily commitment of our female colleagues to helping N-SIDE...
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How digitization has sped up clinical development
The current pandemic has shown an unprecedented transformation in clinical development. While it usually takes up to 10 years to develop, trial and commercialize...
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