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Federal Joint Committee (Germany)

The Federal Joint Committee is the central decision-making body of the self-governing health care system in Germany. Established in 2004 through the merger of several public health agencies, it operates under an independent chairman and a permanent staff.

History
The Federal Joint Committee (G-BA) was formed in 2004 by the merger of the following organizations • Bundesausschuss der Ärzte und Krankenkassen In 2004, they were renamed and merged into the Federal Joint Committee (G-BA) as follows: • Kassenärztliche Bundesvereinigung und Kassenzahnärztliche Bundesvereinigung (National Associations of Statutory Health Insurance Physicians and Dentists) • Deutsche Krankenhausgesellschaft (German Hospital Federation) • GKV-Spitzenverband (Central Federal Association of Health Insurance Funds) As a supreme decision-making body, the Joint Committee exerts a direct influence on the healthcare provisions for millions of people. == Decision-making process ==
Decision-making process
The G-BA is authorized to issue binding regulations based on health reform legislation, along with routine decisions regarding healthcare in Germany. While it is not a subordinate agency and remains independent of the Ministry of Health, the ministry is responsible for legal supervision and reserves the right to review all resolutions and guidelines for final approval or modification. As the supreme decision-making body of the self-governing system—comprising representatives of physicians, dentists, hospitals, sickness funds, and patients—the G-BA determines the benefit package of the statutory health insurance. These directives are legally binding for providers, payers, and approximately 70 million insured persons. == Notable guidelines ==
Notable guidelines
Following the German acupuncture trials from 2002 to 2006, the Committee decided to include acupuncture into the catalogue of services covered by statutory health insurance organizations for the treatment of low back pain and knee pain. On June 17, 2010, the Committee removed the usage of glinides from general prescription guidelines for the reduction of human glucose levels. It justified its decision by referring to the conclusion of the Institute for Quality and Efficiency in Health Care that proof of efficacy was lacking. In 2013, the Committee issued a preliminary decision ruling that a fixed dose combination of Stribild does not offer a benefit over Atripla for HIV treatment. == See also ==
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