A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials Register (EudraCT)
EU's Clinical Trials Regulation and portal goes live 31 January
8 EudraCT
CTIS for authorities - EMA
EudraCT | Clinical trials conduted in the EU need to be registered with the database - Asphalion
What Are the Documents Required for Clinical Trial Applications to Regulatory Authorities in Europe? - Sofpromed
EudraVigilance system overview | European Medicines Agency
EU Health - #HealthUnion a Twitteren: "Guidance on clinical trials during the #COVID19 pandemic, including key changes to: ➡️Distribution of the investigational medicinal products ➡️Monitoring ➡️Remote source data verification (SDV ...
Clinical Trials in the European Union - EMA
Clinical Trials in the European Union - EMA
Cochrane supports European regulators as they urge clinical trial sponsors to share their results | Cochrane
Clinical Trial Regulation — Scendea
New European medical device database may undermine clinical trial transparency
clinical-trials-portal - IDMP1
Flow diagram of the study. Abbreviation: eU-cTr, eU clinical Trials... | Download Scientific Diagram
A brief Introduction on ClinicalTrials.gov (PRS) and EU Clinical Trials Register (EudraCT)
Welcome to CTIS
EMA confirms the EU clinical trial portal and database is fit for purpose
Compliance with requirement to report results on the EU Clinical Trials Register: cohort study and web resource | The BMJ
Health groups urge European universities and hospitals to make their clinical trial results public
Call for all sponsors to publish clinical trial results in EU database | European Medicines Agency
