Ongoing Clinical trials during COVID-19: Common issues and EU regulatory expectations
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: https://www.linkedin.com/events/6673538923479736320/
Presenters : Tessa Fiorini-Cohen and Louise Spencer