Proceedings of the Ninth International Conference of Drug Regulatory Authorities (ICDRA) - Berlin, Germany 25-29 April 1999
(1999; 102 pages) Ver el documento en el formato PDF
Índice de contenido
Abrir esta carpeta y ver su contenidoOpening Ceremony
Abrir esta carpeta y ver su contenidoGood regulatory practice
Abrir esta carpeta y ver su contenidoGood certification practice
Abrir esta carpeta y ver su contenidoCounterfeit drugs: challenges and solutions
Abrir esta carpeta y ver su contenidoCurrent issues in regulation and quality
Abrir esta carpeta y ver su contenidoInternational Conference on Harmonization: implementation and implications
Abrir esta carpeta y ver su contenidoDrug utilization studies
Abrir esta carpeta y ver su contenidoInternational Conference on Harmonization and the common technical document
Abrir esta carpeta y ver su contenidoKeynote address
Abrir esta carpeta y ver su contenidoGlobal and national efforts to reduce tobacco use
Abrir esta carpeta y ver su contenidoElectronic communication in the regulatory process
Cerrar esta carpetaTransparency in monitoring the safety of medicines
Ver el documentoSignal generation
Ver el documentoSafety issues - lessons learnt
Ver el documentoResponse to a drug alert situation
Ver el documentoPrinciples of risk communication
Ver el documentoExisting mechanisms of information exchange
Ver el documentoRecommendations
Abrir esta carpeta y ver su contenidoPharmaceutical products for use in special groups
Abrir esta carpeta y ver su contenidoNeed for Bioequivalence
Abrir esta carpeta y ver su contenidoAntimicrobial resistance: battling the bugs
Abrir esta carpeta y ver su contenidoSafety issues of plasma-derived medicinal products
Abrir esta carpeta y ver su contenidoHerbal medicines
Abrir esta carpeta y ver su contenidoRegulation and access to essential drugs
Ver el documentoParticipants
Ver el documentoBack cover
 

Principles of risk communication

Dr Ralph Edwards, WHO Collaborating Centre for International Drug Monitoring

A few years ago, the major players in the pharmacovigilance information process met in Erice, Italy. The deliberations from this conference became the Erice Declaration, which sets out the principles of good communication practices.

The Declaration stated that industry, doctors, and patients have different - but not contradictory - points of view when questions of drug safety are at issue. Trust and partnerships among the groups was considered important, and a wider public debate was deemed desirable in order to help the public better understand risk. Crisis management is also an important matter where communication plays a major role. Several aspects of the communication of benefit-risk information were outlined in the Declaration.

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Última actualización: le 3 mayo 2013