Ongoing Clinical trials during COVID-19: Common issues and EU regulatory expectations

published 4 Jun 2020

Will you be joining us at our complimentary webinar?

Join us on Thursday 11th June for a complimentary webinar presented by Real Regulatory team members Tessa Fiorini Cohen and Louise Spencer. The webinar will focus on the impact of COVID-19 on ongoing clinical trials within the EU and related regulatory expectations. Risk assessment and regulatory reporting requirements will also be tackled through specific examples encountered by RRL.

Register here:

Presenters : Tessa Fiorini-Cohen and Louise Spencer

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