EU/EC - MEDDEV 2.7/3
GUIDELINES ON MEDICAL DEVICES CLINICAL INVESTIGATIONS: SERIOUS ADVERSE EVENT REPORTING UNDER DIRECTIVES 90/385/EEC AND 93/42/EEC.
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| Organization: | EU/EC |
| Publication Date: | 1 December 2010 |
| Status: | active |
| Page Count: | 6 |
Document History
MEDDEV 2.7/3
December 1, 2010
GUIDELINES ON MEDICAL DEVICES CLINICAL INVESTIGATIONS: SERIOUS ADVERSE EVENT REPORTING UNDER DIRECTIVES 90/385/EEC AND 93/42/EEC.
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