Proceedings of the Tenth International Conference of Drug Regulatory Authorities (ICDRA) - Hong Kong, China, 24 - 27 June 2002
(2002; 166 pages) Voir le document au format PDF
Table des matières
Afficher le documentAbbreviations and acronyms used in this report
Ouvrir ce répertoire et afficher son contenuOpening ceremony
Ouvrir ce répertoire et afficher son contenuHerbal medicines
Ouvrir ce répertoire et afficher son contenuKeynote address
Ouvrir ce répertoire et afficher son contenuSafety of blood-derived products
Ouvrir ce répertoire et afficher son contenuAntimicrobial resistance - new initiatives
Ouvrir ce répertoire et afficher son contenuHarmonization I
Ouvrir ce répertoire et afficher son contenuHarmonization II
Ouvrir ce répertoire et afficher son contenuProtection of trial subjects in clinical trials
Ouvrir ce répertoire et afficher son contenuRegulating biotechnology products
Ouvrir ce répertoire et afficher son contenuRegulatory challenges: health sector reform and drug regulatory capacity
Ouvrir ce répertoire et afficher son contenuAccess to drugs and vaccines I
Ouvrir ce répertoire et afficher son contenuAccess to drugs and vaccines II
Ouvrir ce répertoire et afficher son contenuCounterfeit pharmaceutical products
Ouvrir ce répertoire et afficher son contenuHomoeopathy
Ouvrir ce répertoire et afficher son contenuSafety monitoring
Ouvrir ce répertoire et afficher son contenuE-Commerce
Fermer ce répertoireCurrent topics
Afficher le document“For export only” manufactured drugs and cosmetics that are not legally used in country of manufacture
Afficher le documentWHO Certification Scheme: input for implementation
Afficher le documentValue of joining the Pharmaceutical Inspection Cooperation Scheme (PIC/S) for developing countries: the Malaysian experience
Afficher le documentPharmacopoeial specifications for new drug entities
Afficher le documentImproving the impact of drug regulatory authorities on public health
Afficher le documentStrengthening drug regulatory authorities in small Pacific Island nations
Afficher le documentTransparency of data
Afficher le documentKava
Afficher le documentXenotransplantation and xenotourism: time for concerted regulatory action
Afficher le documentRecommendations
Ouvrir ce répertoire et afficher son contenuRegulatory challenges of new technologies
Afficher le documentList of participants
Afficher le documentBack cover
 

Strengthening drug regulatory authorities in small Pacific Island nations

Mr Peter Zinck, Fiji

The South Pacific Islands comprise 14 countries, including Australia, New Zealand, Papua New Guinea, Samoa, Tonga, Solomon Islands and Fiji. The total population is around 26 million, of whom 20 million are in Australia and New Zealand and 4 million in Papua New Guinea. The remaining 2 million are divided among the other 11 countries.

The regulatory authorities of these small import-oriented countries face many challenges, particularly where gross domestic product is low. Drug budgets are limited, purchasing power is small and it is difficult to source products that are of good quality, reliable and from credible suppliers. Furthermore, because human resources are limited, administrative processes and systems, technical capacity and quality control measures are generally inadequate.

Because of these limitations, DRAs in small Pacific Island nations are exploring the opportunities for regional collaboration in the areas of sharing relevant regulatory information, drug registration, pharmacovigilance and GMP inspection in the hope of strengthening their regulatory capacity. Like New Zealand, which has a strategic alliance with Australia, the small Pacific Island nations are looking for potential twinning arrangements with key regulatory authorities in the region.

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Dernière mise à jour: le 3 mai 2013