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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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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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Why clinical trial timelines are getting longer (and how to fix it)
The development of COVID-19 vaccines in less than a year from when the virus was first sequenced was a monumental achievement. Antiviral medications for COVID...
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How AI & Machine Learning Are Improving Clinical Trial Forecasting
Clinical trials are becoming more complex. New types of therapy like biologics and personalized medicine, as well as treatments targeting rare diseases, create...
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Deep dive into your clinical trial data with the N-SIDE Strategic Dashboard!
Are you struggling to smartly aggregate your clinical supply data ? Do you want to transform this data into actionable insights?
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Join us at Clinical Trial Supply 2020 – Virtual Experience
Join us at the digital edition of the Clinical Trial Supply conference. Due to the COVID-19 situation, the event will be hosted virtually :
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Maximize the supply friendliness of your clinical trial protocol – start optimizing at protocol design!
Critical decisions are taken during protocol design. It is essential to maintain patient centricity and respect site constraints, but it is also an opportunity...
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