Health Industry Manufacturers

C. H. Swanson, Statementfor the Health Industry Manufacturers Association, before the House Government Operations Subcommittee in Information, Justice, Transportation, and Agriculture, Washington, D.C., Oct. 5, 1994. 

A. A. Rosenblatt and J. E. Knapp, Health Industry Manufacturer s Association (HTMAJ Conference Proceedings, 1988, Washington, D.C., pp. 47—50. 

The microbiological studies above are conducted to establish the appropriate dose level to be used to sterilize each specific product or commodity to an acceptable level of statistical nonsterility. These studies should be conducted following qualification of the irradiation facility. The Health Industry Manufacturers Associ-aton (HIMA) [39] has suggested major items to be included in the qualification phase of the validation scheme for radiation sterilization installation. 

Health Industry Manufacturers Association. Medical Device Sterilization Monographs, Sterilization Cycle Development, report no. 78-4.2 (1978). 

Health Industry Manufacturers Association (HIMA), Microbiological evaluation of filters for sterihzing hquids, HIMA Document No.3, Vol. 4, 34 pp., 1982. 

Health Industry Manufacturer s Association (devices) Health Insurance Portability and Accountability Act Indian Health Service Human immunodeficiency vims HIV-positive HIV-infected Human immunodeficiency vims type 1 Health Maintenance Organization... 

Health Industry Manufacturer s Associatk (1982). Microbiologicat Evaluation Filters for Sterilizing Utfuids. HIM A Document No 3. Volume 4. Washington... 

HIMA Health Industry Manufacturers Associa- HUD U.S. Housing and Urban Development... 

A U.S. federal judge s injunction of the FDA s product tracking requirement is issued for secondary wholesalers. Animal health industry manufacturers embrace a global product identification standard. The pharmaceutical industry rushed to meet Turkey s serialization requirements for all products sold in the country. 

SASSUR is targeted at bringing together experts, researchers, and practitioners from diverse communities, such as safety and security engineering, certification processes, model-based technologies, software and hardware design, safety-critical systems, and applications communities (railway, aerospace, automotive, health, industrial manufacturing, etc.). 

Guidance for Industry Manufacturing, Processing, or Holding Active Pharmaceutical Ingredients U.S. Department of Health and Human Services Rockville, MD, 1998. 

Regulatory levels of exposure to various chemicals, among them solvents and benzene, have been a subject for constant pressure from industry manufacturers on one hand, regulatory agencies, health care, and patients on the other hand. The most common question asked is Is there a safe level of exposure to benzene The answer to that question has been given by the American Petroleum Institute in their paper on benzene, 1948, and their statement... 

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