Belgian Health Care Knowledge Centre
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Belgian Health Care Knowledge Centre
The Belgian Health Care Knowledge Centre (abbreviated to KCE) is an independent federal research institute in Belgium that provides multidisciplinary scientific advice to relevant persons and authorities on topics related to health care. More specifically, the KCE carries out research on the organisation and financing of the health system (health services research), assesses health technologies and drugs (health technology assessment), establishes guidelines for clinical practice and updates them according to the latest scientific evidence (good clinical practices), and establishes validated methods for research in the field of health care and public health. Aside from producing scientific reports on these topics, the KCE also maintains a clinical research programme in which it selects and funds non-commercial clinical trials. Lastly, the KCE critically reviews, analyses and summarizes publications from foreign research institutes and peer reviewed journals that could be o ...
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Health Services Research
Health services research (HSR) became a burgeoning field in North America in the 1960s, when scientific information and policy deliberation began to coalesce. Sometimes also referred to as health systems research or health policy and systems research (HPSR), HSR is a multidisciplinary scientific field that examines how people get access to health care practitioners and health care services, how much care costs, and what happens to patients as a result of this care. HSR utilizes all qualitative and quantitative methods across the board to ask questions of the healthcare system. It focuses on performance, quality, effectiveness and efficiency of health care services as they relate to health problems of individuals and populations, as well as health care systems and addresses wide-ranging topics of structure, processes, and organization of health care services; their use and people's access to services; efficiency and effectiveness of health care services; the quality of healthcare ser ...
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Scientific Evidence
Scientific evidence is evidence that serves to either support or counter a scientific theory or hypothesis, although scientists also use evidence in other ways, such as when applying theories to practical problems. "Discussions about empirical evidence have tended to focus on epistemological questions regarding its role in theory testing ... even though empirical evidence also plays important and philosophically interesting roles in other areas including scientific discovery, the development of experimental tools and techniques, and the application of scientific theories to practical problems." Such evidence is expected to be empirical evidence and interpretable in accordance with scientific methods. Standards for scientific evidence vary according to the field of inquiry, but the strength of scientific evidence is generally based on the results of Statistics, statistical analysis and the strength of scientific controls. Principles of inference A person's assumptions or be ...
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Federal Public Service Health (Belgium)
The FPS Public Health, Food Chain Safety and Environment ( nl, FOD Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu, french: SPF Santé publique, Sécurité de la Chaîne alimentaire et Environnement, german: FÖD Volksgesundheit, Sicherheit der Nahrungsmittelkette und Umwelt), more commonly known as the FPS Health, is a Federal Public Service of Belgium. Royal Order established FPS Justice on May 23, 2001, as part of Verhofstadt I Government to rebuild the federal administration. It is responsible for guaranteeing the public health, the safety of the food chain and a safe environment. Organisation The FPS Health is currently organised into three Directorates-General and an Administration: *The Directorate-General for Health Care *The Directorate-General for Animals, Plants and Foodstuffs *The Directorate-General for Environment *The Administration of Medical Expertise (Medex) The former Directorate-General for Medicinal Products has become the autonomous Federal Agenc ...
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National Institute For Health And Disability Insurance
The National Institute for Health and Disability Insurance (NIHDI) is a federal public body of social security in Belgium. Under the authority of the Belgian federal minister of Social Affairs and Public Health, it is responsible for administering the country's compulsory national schemes for health insurance and disability benefits, and manages a compensation fund for medical accidents. Organisation The institute was founded by the law of August 9, 1963 establishing and organizing a scheme for compulsory insurance for medical treatment and benefits, which came into force on January 1, 1964. The law of 1963 has since been replaced by the law of July 14, 1994 regarding the compulsory insurance for medical treatment and benefits coordinated on July 14, 1994. The institute's health and disability insurance budget for 2017 amounted to more than 37 billion euros. Activities * Health insurance: the NIHDI makes rules concerning the reimbursement of costs for health services and es ...
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Health Minister
A health minister is the member of a country's government typically responsible for protecting and promoting public health and providing welfare and other social security services. Some governments have separate ministers for mental health. Country-related articles and lists * Albania: Ministry of Health (Albania) * Argentina: Ministry of Health (Argentina) * Australia: Minister for Health (Australia) * Austria: Minister of Health (Austria) * Azerbaijan: Ministry of Healthcare (Azerbaijan) * Bhutan: Ministry of Health (Bhutan) * Bahamas: Ministry of Health (Bahamas) * Barbados: Ministry of Health and Wellness (Barbados) * Belgium: Ministry of Public Health (Belgium) * Bolivia: Ministry of Health (Bolivia) * Botswana: Ministry of Health and Wellness (Botswana) * Brazil: Ministry of Health (Brazil) * Brunei: Ministry of Health (Brunei) * Cambodia: Ministry of Health, Cambodia * Canada: Minister of Health (Canada) * Chile: Ministry of Health (Chile) * People's Republic of C ...
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Public Law
Public law is the part of law that governs relations between legal persons and a government, between different institutions within a state, between different branches of governments, as well as relationships between persons that are of direct concern to society. Public law comprises constitutional law, administrative law, tax law and criminal law, as well as all procedural law. Laws concerning relationships between individuals belong to private law. The relationships public law governs are asymmetric and inequalized. Government bodies (central or local) can make decisions about the rights of persons. However, as a consequence of the rule-of-law doctrine, authorities may only act within the law (''secundum et intra legem''). The government must obey the law. For example, a citizen unhappy with a decision of an administrative authority can ask a court for judicial review. The distinction between public law and private law dates back to Roman law, where the Roman jurist Ulpian ( ...
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Public Body
A statutory corporation is a government entity created as a statutory body by statute. Their precise nature varies by jurisdiction, thus, they are statutes owned by a government or controlled by national or sub-national government to the (in some cases minimal) extent provided for in the creating legislation. Bodies described in the English language as "statutory corporations" exist in the following countries in accordance with the associated descriptions (where provided). Australia In Australia, statutory corporations are a type of statutory authority created by Acts of state or federal parliaments. A statutory corporation is defined in the government glossary as a "statutory body that is a body corporate, including an entity created under section 87 of the PGPA Act" (i.e. a statutory authority may also be a statutory corporation). An earlier definition describes a statutory corporation as "a statutory authority that is a body corporate", and the New South Wales Governme ...
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Clinician
A clinician is a health care professional typically employed at a skilled nursing facility or clinic. Clinicians work directly with patients rather than in a laboratory or as a researcher. A clinician may diagnose, treat, and otherwise care for patients. For example, psychologists, clinical pharmacists, clinical scientists, nurses, physiotherapists, dentists, optometrists, physician assistants and physicians can be considered clinicians. Many clinicians take comprehensive exams to be licensed and some complete graduate degrees (master's or doctorates) in their field of expertise. A main function of a clinician is to manage a sick person in order to cure the effects of their illness. The clinician can also consider the impact of illness upon the patient and his or her family, as well as other social factors. See also * List of healthcare occupations A listing of health care professions by medical discipline. Anesthesiology * Anesthesiologist * Anesthesiology Fellow * Certifi ...
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Academic Journal
An academic journal or scholarly journal is a periodical publication in which scholarship relating to a particular academic discipline is published. Academic journals serve as permanent and transparent forums for the presentation, scrutiny, and discussion of research. They nearly-universally require peer-review or other scrutiny from contemporaries competent and established in their respective fields. Content typically takes the form of articles presenting original research, review articles, or book reviews. The purpose of an academic journal, according to Henry Oldenburg (the first editor of ''Philosophical Transactions of the Royal Society''), is to give researchers a venue to "impart their knowledge to one another, and contribute what they can to the Grand design of improving natural knowledge, and perfecting all Philosophical Arts, and Sciences." The term ''academic journal'' applies to scholarly publications in all fields; this article discusses the aspects common to all ac ...
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Clinical Trial
Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietary choices, dietary supplements, and medical devices) and known interventions that warrant further study and comparison. Clinical trials generate data on dosage, safety and efficacy. They are conducted only after they have received health authority/ethics committee approval in the country where approval of the therapy is sought. These authorities are responsible for vetting the risk/benefit ratio of the trial—their approval does not mean the therapy is 'safe' or effective, only that the trial may be conducted. Depending on product type and development stage, investigators initially enroll volunteers or patients into small pilot studies, and subsequently conduct progressively larger scale comparative studies. Clinical trials can vary i ...
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Non-commercial
A non-commercial (also spelled noncommercial) activity is an activity that does not, in some sense, involve commerce, at least relative to similar activities that do have a commercial objective or emphasis. For example, advertising-free community radio stations are typically nonprofit organizations staffed by individuals volunteering their efforts to air a wide variety of radio programming, and do not run explicit radio advertisements, included in the United States specific grouping of "non-commercial educational" (NCE) public radio stations. Some Creative Commons license A Creative Commons (CC) license is one of several public copyright licenses that enable the free distribution of an otherwise copyrighted "work".A "work" is any creative material made by a person. A painting, a graphic, a book, a song/lyrics ...s include a "non-commercial" option, which has been controversial in definition.
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Clinical Research
Clinical research is a branch of healthcare science that determines the safety and effectiveness ( efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical research is different from clinical practice. In clinical practice established treatments are used, while in clinical research evidence is collected to establish a treatment. Overview The term "clinical research" refers to the entire bibliography of a drug/device/biologic, in fact any test article from its inception in the lab to its introduction to the consumer market and beyond. Once the promising candidate or the molecule is identified in the lab, it is subjected to pre-clinical studies or animal studies where different aspects of the test article (including its safety toxicity if applicable and efficacy, if possible at this early stage) are studied. In the United States ...
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