TELAH TERBIT GUIDELINES EDISI KE-3...!!!
A patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes.
A registry database is a file (or files) derived from the registry. Although registries can serve many purposes: to describe the natural history of disease, to determine clinical effectiveness or cost effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care.
While many countries struggle with the consequences and problems of communicable diseases, chronic noncommunicable diseases are on the rise. In addition to being a major cause of death, many surviving ...
Penderita Stroke Akan Didata
SEMARANG. KOMPAS - Mulai tahun 2013, penderita stroke akan didata melalui seluruh rumah sakit di Indonesia. Pendataan dibutuhkan untuk mendapatkan angka penderita stroke ...
20 items in the Registration Data Set
The minimum amount of trial information that must appear in a register in order for a given trial to be considered fully registered.
1. Primary Registry and T ...
INDONESIA AKAN MELAKUKAN "JAMU REGISTRY"
Integrasi pelayanan kesehatan tradisional dalam pelayanan kesehatan formal merupakan suatu program pemerintah utamanya ...