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Areas covered by the Radiation Exposure Compensation Program. The United States Radiation Exposure Compensation Act (RECA) is a federal statute implemented in 1990, set to expire in July 2024, providing for the monetary compensation of people, including atomic veterans, who contracted cancer and a number of other specified diseases as a direct result of their exposure to atmospheric nuclear ...
In July 2001, nine Energy Employee Compensation Resource Centers were opened as a joint initiative of Departments of Labor and Energy. They were staffed and resourced to assist workers and their families with the lodgement of claims. The Department of Energy was to provide exposure data and work documentation. [6]
Importantly, second opinions in or out of network for all cancer patients were also included, so that any cancer patient would have coverage to visit a major cancer center if they chose. In an additional breakthrough, self-insured plans were also subject to these mandates. The history of the law is an interesting one.
(Reuters) -A U.S. appeals court on Friday refused to block a federal mandate requiring health insurers to cover preventive care services like cancer screenings and HIV-preventing medication at no ...
The Clinical Laboratory Improvement Act of 1988 (CLIA 88) was passed in the USA subsequent to the publication of an article in November 1987 in The Wall Street Journal entitled "Lax Laboratories: The Pap Test Misses Much Cervical Cancer Through Labs Errors", which alerted the public to the fact that a pap smear may be falsely negative.
Medicare coverage of colonoscopies and other colorectal cancer screening tests Colonoscopy. If you’re at high risk for colorectal cancer, Medicare covers screening colonoscopies once every 24 ...
A Michigan lawmaker has introduced new legislation, moved by a Scripps News and ProPublica joint investigation into the insurance company that denied a man coverage of cancer treatment, despite ...
Right-to-try laws are United States state laws and a federal law that were created with the intent of allowing terminally ill patients access to experimental therapies (drugs, biologics, devices) that have completed Phase I testing but have not been approved by the Food and Drug Administration (FDA). Prior to the passage of right to try laws ...