eCTD publishing & eSubmissions | Solutions

May 8, 2023

Have a look at this infographic to see how Asphalion´s expertise on eCTD publishing and eSubmissions can help you with your regulatory processes. We have a team devoted to Data Management and eSubmission that uses the latest regulatory intelligence technologies and, that can provide you with successful, high-quality support for your projects.


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NEW | User Acceptance Testing (UAT) phase

Asphalion Expert Beatriz Ugalde Dionicio has been selected by the European Medicines Agency (EMA) to participate in the Product Management Service (PMS) Product User Interface

NEW | CTIS EMA Subject Matter Expert

At Asphalion we are very proud to announce that Nuria Garcia Pazos has been appointed EMA Subject Matter Expert (SME) for Clinical Trials Information System

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