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Biotech Clinical Development in European Union Anticipating the regulatory hurdles

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With the exponential growth in biotechnology product development, it follows that there is a corresponding increase in biotech clinical trial experience. However, despite this increase in experience, biotech clinical development continues to be a challenging exercise, particularly anticipating the regulatory requirements for gaining approval to conduct a trial and later the clinical requirements for marketing approval.

Stuart Mudge, Emmanuelle Voisin

2003 – Applied Clinical trials
Biotech Clinical Development in European Union : Anticipating the regulatory hurdles

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    publication by

    Emmanuelle M. Voisin, PhD
    Emmanuelle M. Voisin, PhD
    Founder and CEO
    Dr. Emmanuelle Voisin founded Voisin Consulting Life Sciences (VCLS) in 1997. The firm has become a leading advisor to Biotech,…
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