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Technical Files and Design Dossiers for Medical Devices |
AMP Technology Centre, Sheffield |
01/May/2014
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2 |
More information and booking |
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Investigating Out of Specification Results |
Manchester Marriott Victoria and Albert Hotel, Manchester, UK |
02/May/2014
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1 |
More information and booking |
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QP Module 10: Practical Module (Formulation, Manufacturing, Analysis) |
The University of Strathclyde, Glasgow, Scotland, UK |
12/May/2014
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5 |
More information and booking |
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Effective Pharmaceutical Audits and Self-Inspections (An IRCA Certified Pharmaceutical QMS Auditor/Lead Auditor Course) |
Manchester Marriott Victoria and Albert Hotel, Manchester, UK |
19/May/2014
|
5 |
More information and booking |
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Quality System Product Realisation Process & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
19/May/2014
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1/2 |
More information and booking |
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ISO 13485 Quality System Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
19/May/2014
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1/2 |
More information and booking |
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Quality System Top Management Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
20/May/2014
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1/2 |
More information and booking |
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Quality System Resource Management Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
20/May/2014
|
1/2 |
More information and booking |
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Quality System CAPA & Improvement Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
21/May/2014
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1/2 |
More information and booking |
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Managing Suppliers within a Quality Management System Framework for Medical Devices |
AMP Technology Centre, Sheffield |
21/May/2014
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1/2 |
More information and booking |
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Medical Device Process Validation |
AMP Technology Centre, Sheffield |
22/May/2014
|
1 |
More information and booking |
An NSF International Company 