2011-06-05-世界卫生组织-Glossary_58页_339kb

This glossary is a comprehensive collection of definitions and explanations related to pharmaceuticals, healthcare regulations, economic aspects of medicine, global health issues, and organizational frameworks. It includes terms such as accreditation, adverse drug reactions, antimicrobial resistance, clinical trial phases, compulsory licensing, WTO TRIPS Agreement, essential medicines, and ethical considerations in healthcare. Authored and sourced from organizations like WHO, OECD, and UN agencies, it serves as an authoritative resource for understanding health systems, drug safety, and public health policies. Key themes cover quality assurance, pharmacovigilance, pricing mechanisms, and international cooperation in medicine development and distribution. The content highlights the integration of scientific, legal, and economic perspectives to promote safe and affordable healthcare globally.