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3. Device regulation in the European Union: response from MHRA. Woods K. Lancet; 2012 Feb 11; 379(9815):515. PubMed ID: 22285054 [No Abstract] [Full Text] [Related]
4. Industrial, scientific and medical equipment: proposed rulemaking. Fed Regist; 1978 Oct 06; 43(195):46326-49. PubMed ID: 10238660 [No Abstract] [Full Text] [Related]
5. Safety by design in electromedical equipment: Part I. Loznen SP. Med Device Technol; 1995 Nov 06; 6(9):24-30. PubMed ID: 10158129 [Abstract] [Full Text] [Related]
6. Provision of a microbiological device evaluation service. Perry KR. Commun Dis Public Health; 2004 Mar 06; 7(1):86-8. PubMed ID: 15137289 [No Abstract] [Full Text] [Related]
8. The inevitable metric advance. Elwell R. Am Educ; 1976 Dec 06; 12(10):6-9. PubMed ID: 10243761 [No Abstract] [Full Text] [Related]
9. [Medical device evaluation: what are the needs?]. Huot L, Decullier E, Aulagner G, Chapuis FR. Presse Med; 2010 Oct 06; 39(10):1097-8. PubMed ID: 20634034 [No Abstract] [Full Text] [Related]
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