WEBINAR RECORDING | Reactivation of EMA Policy 0070: Introduction and key recommendations for a successful Publication

November 23, 2023

Watch Asphalion experts Ivette Camarasa and Nuria García Pazos in this webinar talking about EMA Policy 0070 and sharing key recommendations for a successful publication.

We would like to thank everyone for the interest shown in our webinars and we look forward to sharing much more knowledge and experience with our audience.

New webinar coming soon -> November, 30. “Digitalization trends in Pharmacovigilance: How does digitalization impact routine pharmacovigilance activities and what to expect in the near future?”.

You can now watch the Reactivation of EMA Policy 0070: Introduction and key recommendations for a successful Publication Webinar here:

REACTIVATION OF EMA POLICY 0070 WEBINAR

For further information, please feel free to contact us at: info@asphalion.com

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CTIS is the single-entry point for the submission and assessment of clinical trial applications in the EU. It features a public, searchable database aimed at delivering a high level of transparency. The authorisation and oversight of clinical trials are managed by EU/EEA Member States, while the EMA maintains the CTIS. The European Commission oversees the implementation of the Clinical Trials Regulation.

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