Centralize, Modernize, Harmonize: The Acceleration of Regulatory Digital Trends Journal Article 27th March 2024
FDA clarifies use of Clinical Data in Premarket Notification Submissions Blog & Article 22nd March 2024
Webinar IRIS Portal – Scientific Advice, Orphan Designation, and i-SPOC application submissions to EMA 3rd November 2022
Webinar What you need to know to submit Study Data to FDA & what the new FDA Technical Rejection Criteria means for you