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What is a clinical trial supply risk management plan?

When we talk about risk management in clinical trial supply, we’re usually referring to two types of risk:

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Meet N-SIDE’s Team of Experts on Oncology Clinical Trials

Interview by N-SIDE’s Growth Marketing Coordinator, Donokhon Abulkasimova    Did you know that N-SIDE has a special team of experts, who power innovation in...

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Join us at Arena CTS Nordics in Copenhagen!

Will we see you at Arena CTS Nordics next October?  Join us and meet our Life Sciences experts October 25th and 26th at Arena CTS Nordics in Copenhagen. Our...

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Meet our experts at Arena CTS East Coast

Our experts are attending Arena Clinical Trial Supply East Coast! You can meet our Life Sciences team October 19th and 20th October at Arena CTS East Coast in...

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Join N-SIDE's showcase at the GCSG 2022 European Knowledge Forum!

Our Life Sciences team will be at the GCSG 2022 European Knowledge Forum! You can meet our experts from October 4th until October 6th at the GSCG EKF 2022 in...

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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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