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Guidance note for the registration of persons responsible for placing devices on the market in accordance with Directive 93/42/EEC and S.I. No. 252 of 1994
Irish Medicines Board (IMB)
Irish Medicines Board (IMB)
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Author
Advisors
Editors
Other Contributors
Departments
Date
2004-10-21
Date Submitted
Keywords
MEDICAL DEVICES
REGULATION
REGULATION
Other Subjects
Subject Mesh
Planned Date
Start Date
Collaborators
Principal Investigators
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IMB 2004
Adobe PDF, 150.77 KB
Alternative Titles
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Abstract
Language
en
