Suchergebnisse - "van der Elst, Menno"

PubPharm (22)

1

The Role of the European Medicines Agency in the Safety Monitoring of COVID-19 Vaccines and Future Directions in Enhancing Vaccine Safety Globally

enthalten in: Drug safety | 2024

von Caplanusi, I. | Szmigiel, A. | van der Elst, M. | +6

2

The Role of the European Medicines Agency in the Safety Monitoring of COVID-19 Vaccines and Future Directions in Enhancing Vaccine Safety Globally

enthalten in: Drug safety | 2024

von Caplanusi, I. | Szmigiel, A. | van der Elst, M. | +6

3

Predicting the submission frequency of periodic safety update reports : development and application of the EURD tool

enthalten in: Frontiers in medicine | 2024

von Gordillo-Marañón, M. | Candore, G. | López-Fauqued, M. | +7

4

The Role of Regulator-Imposed Post-Approval Studies in Health Technology Assessments for Conditionally Approved Drugs

enthalten in: International journal of health policy and management | 2022

von Vreman, R. | Bloem, L. | van Oirschot, S. | +6

5

Pre-approval and post-approval availability of evidence and clinical benefit of conditionally approved cancer drugs in Europe : A comparison with standard approved cancer drugs

enthalten in: British journal of clinical pharmacology | 2022

von Bloem, L. | Bot, R. | Mantel-Teeuwisse, A. | +5

6

Comprehensive evaluation of post-approval regulatory actions during the drug lifecycle - a focus on benefits and risks

enthalten in: Expert opinion on drug safety | 2021

von Bloem, L. | Karomi, M. | Hoekman, J. | +4

7

Associations between uncertainties identified by the European Medicines Agency and national decision making on reimbursement by HTA agencies

enthalten in: Clinical and translational science | 2021

von Bloem, L. | Vreman, R. | Peeters, N. | +6

8

Comprehensive evaluation of post-approval regulatory actions during the drug lifecycle – a focus on benefits and risks

enthalten in: Expert opinion on drug safety | 2021

von Bloem, L. | Karomi, M. | Hoekman, J. | +4

9

Impact of safety-related regulatory action on clinical practice : a systematic review

enthalten in: Drug safety | 2012

von Piening, S. | Haaijer-Ruskamp, F. | de Vries, J. | +4

10

Impact of Safety-Related Regulatory Action on Clinical Practice: A Systematic Review

enthalten in: Drug safety | 2012

von Piening, S. | Haaijer-Ruskamp, F. | de Vries, J. | +4