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Nicolas Rouillé on Muck Rack

Nicolas Rouillé

As seen in: Clinical Leader
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Articles

Metadata Repositories: Overcoming Challenges with Automation

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By Angelo Tinazzi, Nicolas Rouillé, Sebastià Barceló
| cytel.com
CDISC| data submission| metadata | Written by Angelo Tinazzi, Nicolas Rouillé, and Sebastià Barceló In the realm of standards management, companies of all sizes are increasingly exploring the potential of metadata repositories (MDR). From protocol development to eCRF, SDTM, and ADaM to Analysis Results, these repositories are being used to speed up study set up and delivery.
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11.16.20 -- Getting A Handle On Clinical Trial Costs

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By Cynthia Schnedar, Kate Cook, Nicolas Rouillé, Eric Henniger
| Clinical Leader Verified
Newsletter | November 16, 2020 By Amit Pratap Singh Rathore, principal analyst, Beroe Inc. Recently, clinical trials have become very complex affairs, especially for small and midsize biotech companies. There are many factors behind this, including, but not limited to, increased costs and regulatory requirements. According to Tomasz Sablinski, CEO at Transparency Life Sciences, the cost of clinical trials increased by around 100 percent from 2008 to 2019.
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