Food and Drug Administration Center for Devices and Radiological Health. Guidance for Magnetic Resonance Diagnostic Devices. Criteria for Significant Risk Investigation1997.
2.
Food and Drug Administration Center for Devices and Radiological Health, “Criteria for Significant Risk Investigations of Magnetic Resonance Diagnostic Devices”2003.
3.
Comitato Elettrotecnico Italiano, Apparecchi Elettromedicali Parte 2: Prescrizioni particolari d sicurezza relative agli apparecchi a risonanza magnetica per diagnostica medica. CEI EN 60601-2-33/A11 1998.
4.
International Electrotechnical Commission. “Medical electrical equipment. Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis”. IEC 60601 1-2-33 Ed. 2.0 2002.
5.
International Commission for non Ionizing Radiation Protection, “Guidelines on limits of exposure to static magnetic fields”Health Physics Society66: 100–1061994.