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1. Experiences and challenges with the new European Clinical Trials Regulation.

2. Evaluating the re-identification risk of a clinical study report anonymized under EMA Policy 0070 and Health Canada Regulations.

3. Expanded Access Programme: looking for a common definition.

4. Through the looking glass: understanding non-inferiority.

5. Outcome selection for tissue-agnostic drug trials for immune-mediated inflammatory diseases: a systematic review of core outcome sets and regulatory guidance.

6. A narrative review of estimands in drug development and regulatory evaluation: old wine in new barrels?

7. Effect and safety of 4% albumin in the treatment of cardiac surgery patients: study protocol for the randomized, double-blind, clinical ALBICS (ALBumin In Cardiac Surgery) trial.

8. Monitoring in practice - How are UK academic clinical trials monitored? A survey.

9. Adaptive designs in clinical trials: from scientific advice to marketing authorisation to the European Medicine Agency.