EMA confirms the EU clinical trial portal and database is fit for purpose
SUSAR reporting | Icelandic Medicines Agency
Comparison of regulatory pathways for the approval of advanced therapies in the European Union and the United States - Cytotherapy
Call for all sponsors to publish clinical trial results in EU database | European Medicines Agency
EU Medicines Agency on Twitter: "In a letter published today, @EU_Commission, #EMA and the Heads of Medicines Agencies remind all sponsors of #ClinicalTrials conducted in the 🇪🇺 to make results of concluded
Assessment of the Regulatory Dialogue Between Pharmaceutical Companies and the European Medicines Agency on the Choice of Noninferiority Margins - Clinical Therapeutics
Welcome to CTIS
EudraVigilance system overview | European Medicines Agency
Material and information about the upcoming CTIS from EMA – Ascro
Clinical Trials in the European Union - EMA
EU CTR Frequently Asked Questions
Cell-free DNA analysis in current cancer clinical trials: a review | British Journal of Cancer
Approval rating: how do the EMA and FDA compare? | Cancer World Archive
New Clinical Trials Information System - NREC
What are the EMA Guidelines for Clinical Trial Management? – pepgra
Approval rating: how do the EMA and FDA compare? | Cancer World Archive
CTIS for sponsors - EMA
EU's Clinical Trials Regulation and portal goes live 31 January
Clinical data publication | European Medicines Agency
clinical-trials-portal - IDMP1
Clinical Trial Regulation Update - PharSafer® - Specialists in Global Clinical and Post Marketing Drug Safety
Session 2 - Update on implementation of CTR - A.M. Janson Lang
Clinical Trial Disclosure: Summary of the main requirements in EU/EEA... | Download Table
