Asphanews November 2016
We are proud to announce that the Spanish Government has granted us the seal of Innovative SME
Are you considering to carry out a Scientific Advice meeting with the European Medicines Agency?
Now is the time to plan ahead! EMA has already released the timelines for 2017. In Asphalion we can support you with setting-up the strategy and preparing your Briefing Package, as well as accompany you to the formal meeting.
Fast Product’s Registration in SFDA
Saudi Arabia FDA (SFDA) is adopting a new product registration mechanism from 1st February 2017. Thanks to this new procedure, the registration decision is shorten to either 30 or 60 days. Asphalion can be the perfect support for the procedure!
Biospain Press Conference
Asphalion participations in H2020 programme were explained in detail by our General Manager in Regulatory Affairs, Lidia Cánovas, in the press conference and in a radio interview at BioSpain 2016 in Bilbao.
Effective data management for benefits beyond compliance with IDMP!
Our director of Regulatory Information, Remco Munnik, is one of the distinguished speakers in the upcoming CBI’s 2nd Annual IDMP Update Forum event in Philadelphia on Dec 8-9. As an expert, he will present the latest developments of ISO IDMP and the impact on Industry. If you are interested, you can still joint the event! Read more