Clinical Trials

YDL Ventures offers a One-Stop Shop for clinical trials through its partners at Eurofins Optimed. With over 25 years of experience, Eurofins is a worldwide leader in early clinical trials.

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According to your needs, Eurofins can manage all the steps of your trial in Europe including study document design, regulatory requirements, study conduct, monitoring, pharmaceutical operations, bioanalysis, data collection & biometry, and report writing.

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Focused on early clinical development, our experience of more than 1,000 trials conducted since our creation establishes Eurofins Optimed as a reliable partner. We are able to provide you with GCP services in any therapeutic field thanks to an experienced team of experts and our large network of Key Opinion Leaders.

As every clinical project is specific, we offer tailor-made solutions among the following activities:

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• Study document development: protocol, ICF, e-CRF, diaries, IMPD

•  Regulatory support and submissions in Europe and in the USA

• Clinical Investigations: in our Clinical Pharmacology Unit (France – 60 beds) or through our network of Investigators within Europe and the USA

• Support services: feasibility studies (site identification and qualification), project management, site coordination, monitoring

•  Data collection and analysis: data management, statistics, e-CRF, medical writing, ePro

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