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Structure of the Regulatory Agencies for Medical Devices |
AMP Technology Centre, Sheffield |
07/Jul/2014
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1 |
More information and booking |
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Pre Market Technical Briefings for Medical Devices |
AMP Technology Centre, Sheffield |
08/Jul/2014
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2 |
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Regulatory Agency Enforcement & Remediation for Medical Devices |
AMP Technology Centre, Sheffield |
10/Jul/2014
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2 |
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Medical Device Research Methods |
AMP Technology Centre, Sheffield |
14/Jul/2014
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1 |
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Qualified Person Role & Responsibility for Medical Devices |
AMP Technology Centre, Sheffield |
15/Jul/2014
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1 |
More information and booking |
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QP Module 12: The Role and Professional Duties of the Qualified Person |
Hilton York Hotel, York, UK |
21/Jul/2014
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4 |
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EU Medical Device CE Marking - Understanding |
AMP Technology Centre, Sheffield |
21/Jul/2014
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1 |
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EU Medical Device CE Marking - Implementing |
AMP Technology Centre, Sheffield |
22/Jul/2014
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2 |
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EU Medical Device CE Marking - Advanced |
AMP Technology Centre, Sheffield |
24/Jul/2014
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2 |
More information and booking |
An NSF International Company 