INTRODUCTION: Previous studies have found differences in the communication of safety issues among medicines regulatory agencies.OBJECTIVES: To explore (1) to what extent regulators' opinions regarding the need to communicate safety issues related to sodium-glucose cotransporter-2 (SGLT2) inhibitors might be influenced by their concern about the safety issue, and (2) whether regulators' concerns might be influenced by certain characteristics of the safety issue or by the demographic and professional characteristics and attitudes of the regulators.METHODS: An online cross-sectional survey study with a rating-based conjoint analysis among clinical and pharmacovigilance assessors from the EU regulatory network was performed between April and Ju...
Over the past 10years, European pharmaceutical regulators (especially the European Medicines Agency ...
Background: After market approval, new serious safety issues are regularly identified for drugs that...
Background: As pre-approval trials are inherently limited in assessing the complete benefit-risk pro...
INTRODUCTION: Previous studies have found differences in the communication of safety issues among me...
Background Information about the safety of medicines often emerges after approval. Medicines’ regul...
Introduction Healthcare professionals (HCPs) are informed about new drug safety issues through Direc...
Aims: Regulatory risk communications are important to ensure medication safety, but their impact is ...
National competent authorities (NCAs) use Direct Healthcare Professional Communications (DHPCs) to c...
Over the past 10 years, European pharmaceutical regulators (especially the European Medicines Agency...
Introduction: When serious medication errors (ME) are identified, communication to the field may be ...
Background: After market approval, new serious safety issues are regularly identified for drugs that...
BACKGROUND: As pre-approval trials are inherently limited in assessing the complete benefit-risk pro...
Over the past 10years, European pharmaceutical regulators (especially the European Medicines Agency ...
Background: After market approval, new serious safety issues are regularly identified for drugs that...
Background: As pre-approval trials are inherently limited in assessing the complete benefit-risk pro...
INTRODUCTION: Previous studies have found differences in the communication of safety issues among me...
Background Information about the safety of medicines often emerges after approval. Medicines’ regul...
Introduction Healthcare professionals (HCPs) are informed about new drug safety issues through Direc...
Aims: Regulatory risk communications are important to ensure medication safety, but their impact is ...
National competent authorities (NCAs) use Direct Healthcare Professional Communications (DHPCs) to c...
Over the past 10 years, European pharmaceutical regulators (especially the European Medicines Agency...
Introduction: When serious medication errors (ME) are identified, communication to the field may be ...
Background: After market approval, new serious safety issues are regularly identified for drugs that...
BACKGROUND: As pre-approval trials are inherently limited in assessing the complete benefit-risk pro...
Over the past 10years, European pharmaceutical regulators (especially the European Medicines Agency ...
Background: After market approval, new serious safety issues are regularly identified for drugs that...
Background: As pre-approval trials are inherently limited in assessing the complete benefit-risk pro...