Year: 2005
Language: Arabic
This resource is also available in: الإنجليزية الفرنسية الروسية الأسبانية الصينية المبسطة
Author(s): Bruce Evatt
Format: Document
Having a national patient registry means being able to answer fundamental questions about the hemophilia population within a given country. This step-by-step guide outlines the basic principles of data collection, maintenance, and analysis and compares different types of registries.
ستدور عروض ومناقشات النسخة الثانية من القمة العالمية للسياسات والقدرة على الوصول للاتحاد العالمي للهيموفيليا حول تحسين الرعاية و الحصول
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