Sabine J. Straus
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 72 publications
European Medicines Agency seeks stakeholders' views on its reflection paper on patient experience data.
Journal: British journal of clinical pharmacology
Published: October 17, 2025
Applying the EU Regulatory Framework to Determine the Benefit-Risk Profile of Psychedelics.
Journal: ACS pharmacology & translational science
Published: June 25, 2025
Risk Minimisation Measures of Advanced Therapy Medicinal Products Authorised in the EU Between 2009 and 2023: A Cross-Sectional Study.
Journal: Drug safety
Published: March 31, 2025
Meningococcal B Vaccines as a Paradigm of Safe and Effective Vaccines for Children.
Journal: Vaccines
Published: February 26, 2025
Optimizing Patient Registries for Regulatory Decision Making - Key Learnings From an HMA/EMA Multistakeholder Workshop.
Journal: Clinical pharmacology and therapeutics
Published: December 05, 2024
Commentary/Response to Damkier et al.
Journal: Pharmacoepidemiology and drug safety
Published: October 31, 2024
Duration of Time Intervals for Risk Minimization Measure Effectiveness Studies.
Journal: Clinical pharmacology and therapeutics
Published: September 13, 2024
The Role of the European Medicines Agency in the Safety Monitoring of COVID-19 Vaccines and Future Directions in Enhancing Vaccine Safety Globally.
Journal: Drug safety
Published: February 04, 2024
Studying the Impact of European Union Regulatory Interventions for Minimising Risks From Medicines: Lessons Learnt and Recommendations.
Journal: Pharmacoepidemiology and drug safety
Published: January 12, 2024
Real-World Evidence to Support EU Regulatory Decision Making-Results From a Pilot of Regulatory Use Cases.
Journal: Clinical pharmacology and therapeutics
Published: January 11, 2024
Last Updated: 09/26/2026