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

published 16 Jun 2020

Due to the success of our recent webinar, we shall be running it again. We hope you can join us!

Will you be joining us at our complimentary webinar?

Join us on Thursday 18th 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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