As seen on European Pharmaceutical Contractor - Posted Aug. 14, 2019
Aug. 14, 2019 | By Thomas Wicks | The way clinical trials are conducted in the EU will undergo a major change when the clinical trial regulation comes into application, and time is running out for clinical trial sponsors to prepare.
The European Medicines Agency is developing a new clinical trial information system (CTIS) that will provide a single portal for submitting and managing clinical trial application (CTA) dossiers, authorizations, and transparency.
This article is taken from European Pharmaceutical Contractor August 2019, pages 36-37.
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