Have a look at a recent success story of how Asphalion prepared and submitted an NDA application to the FDA for a Swiss Pharmaceutical company with a very tight submission calendar.
Thanks to our extensive track record of over 20 year at Asphalion we can assist you with your eSubmissions to the FDA, EMA, etc. and with all other kind of projects.
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Seamless Regulatory Submissions Meeting Global Standards
Test your Regulatory knowledge!! The summer is back and, for a 4th year in a row, so is Asphalion’s classic ASPHAQUIZ on LinkedIn, our daily
On 18th June 2024, a new version 3.1 of the EU eCTD M1 specification was published on the eSubmission website, marking a significant milestone in
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