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M13 - Process Validation Professional - Process Validation for Medical Devices – Planning and Conducting |
AMP Technology Centre, Sheffield |
07/Jul/2015
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3 |
More information and booking |
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M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software Regulatory Requirements - Step by Step |
AMP Technology Centre, Sheffield |
13/Jul/2015
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1 |
More information and booking |
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M3 - CE & Global Clinical Requirements - Planning and Conducting Clinical Investigations for Medical Devices |
AMP Technology Centre, Sheffield |
13/Jul/2015
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1 |
More information and booking |
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M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software - Technical File and Quality System Requirements |
AMP Technology Centre, Sheffield |
14/Jul/2015
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2 |
More information and booking |
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M3 - CE & Global Clinical Requirements - Medical Devices Clinical Evaluation - Step by Step (QP) |
AMP Technology Centre, Sheffield |
14/Jul/2015
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2 |
More information and booking |
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M3 - CE & Global Clinical Requirements - Post Market Clinical Follow Up for Medical Devices (QP) |
AMP Technology Centre, Sheffield |
16/Jul/2015
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2 |
More information and booking |
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M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software Regulatory Requirements - Step by Step |
AMP Technology Centre, Sheffield |
16/Jul/2015
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1 |
More information and booking |
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M12 - Supplier Quality Professional - Understanding Supplier Control for Medical Devices – CE Marking |
AMP Technology Centre, Sheffield |
20/Jul/2015
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1 |
More information and booking |
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M12 - Supplier Quality Professional - Implementing Supplier Control for Medical Devices – CE Marking |
AMP Technology Centre, Sheffield |
21/Jul/2015
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2 |
More information and booking |