Proceedings of the Ninth International Conference of Drug Regulatory Authorities (ICDRA) - Berlin, Germany 25-29 April 1999
(1999; 102 pages) Voir le document au format PDF
Table des matières
Ouvrir ce répertoire et afficher son contenuOpening Ceremony
Ouvrir ce répertoire et afficher son contenuGood regulatory practice
Ouvrir ce répertoire et afficher son contenuGood certification practice
Ouvrir ce répertoire et afficher son contenuCounterfeit drugs: challenges and solutions
Ouvrir ce répertoire et afficher son contenuCurrent issues in regulation and quality
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization: implementation and implications
Ouvrir ce répertoire et afficher son contenuDrug utilization studies
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization and the common technical document
Ouvrir ce répertoire et afficher son contenuKeynote address
Ouvrir ce répertoire et afficher son contenuGlobal and national efforts to reduce tobacco use
Ouvrir ce répertoire et afficher son contenuElectronic communication in the regulatory process
Ouvrir ce répertoire et afficher son contenuTransparency in monitoring the safety of medicines
Ouvrir ce répertoire et afficher son contenuPharmaceutical products for use in special groups
Ouvrir ce répertoire et afficher son contenuNeed for Bioequivalence
Fermer ce répertoireAntimicrobial resistance: battling the bugs
Afficher le documentCountry experience in implementing antimicrobial resistance strategies
Afficher le documentVeterinary, aquaculture and agricultural use’ of antimicrobials contributing to resistance
Afficher le documentThe role of regulators in the containment of resistance
Afficher le documentRecommendations
Ouvrir ce répertoire et afficher son contenuSafety issues of plasma-derived medicinal products
Ouvrir ce répertoire et afficher son contenuHerbal medicines
Ouvrir ce répertoire et afficher son contenuRegulation and access to essential drugs
Afficher le documentParticipants
Afficher le documentBack cover
 

Recommendations

As part of WHO’s global strategy for the containment of resistance to antimicrobial drugs, and in collaboration with Member States, WHO is invited to:

1. Bring together national authorities for human and veterinary drug regulation to exchange information and to consider joint action.

2. Provide guidance on the clinical development of antimicrobial drugs, in particular to optimize efficacy while minimizing the risk of resistance.

3. Establish a common format for product information and patient information leaflets, specifically addressing antimicrobial resistance issues such as specifications for medicines, susceptibility of common pathogens and measures to prevent resistance. Special attention should be given to improving the communicative potential of the information provided. This information should be regularly updated in the light of prevailing resistance patterns.

4. Continue efforts, as set out in WHO resolution WHA 51.17, to make antimicrobial drugs available on a prescription-only basis.

5. Stimulate drug regulatory authorities to share all relevant information on clinical trials involving antimicrobial drugs, with public health authorities.

 

vers la section précédente vers la section suivante
 

Dernière mise à jour: le 3 mai 2013