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Understanding Design Control for Medical Devices |
AMP Technology Centre, Sheffield |
17/Feb/2014
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1 |
More information and booking |
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Implementing Design Control for Medical Devices |
AMP Technology Centre, Sheffield |
18/Feb/2014
|
1 |
More information and booking |
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Understanding Risk Management - ISO14971 for Medical Devices |
AMP Technology Centre, Sheffield |
19/Feb/2014
|
1 |
More information and booking |
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Understanding Product Validation for Medical Devices |
AMP Technology Centre, Sheffield |
20/Feb/2014
|
1 |
More information and booking |
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Introduction to Post Market Surveillance and Vigilance for Medical Devices |
AMP Technology Centre, Sheffield |
17/Mar/2014
|
1 |
More information and booking |
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Post Market Surveillance and Vigilance for Medical Devices |
BIVDA (LONDON) |
18/Mar/2014
|
2 |
More information and booking |
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A practical overview of the revision to the IVD Directive 98/79/EC |
Scottish LifeSciences Association |
20/Mar/2014
|
1 |
More information and booking |
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Planning and Conducting Clinical Investigations for Medical Devices |
AMP Technology Centre, Sheffield |
24/Mar/2014
|
1 |
More information and booking |
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Medical Devices Clinical Evaluation – Step by Step |
AMP Technology Centre, Sheffield |
25/Mar/2014
|
2 |
More information and booking |
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Post Market Clinical Follow up for Medical Devices |
AMP Technology Centre, Sheffield |
27/Mar/2014
|
2 |
More information and booking |
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World Wide Quality and Regulatory for Medical Devices |
AMP Technology Centre, Sheffield |
31/Mar/2014
|
2 |
More information and booking |
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Medical Device Project Management |
AMP Technology Centre, Sheffield |
08/Apr/2014
|
1 |
More information and booking |
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The Design History File for Medical Devices |
AMP Technology Centre, Sheffield |
28/Apr/2014
|
1 |
More information and booking |
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Writing Technical Summaries for Medical Devices |
AMP Technology Centre, Sheffield |
29/Apr/2014
|
2 |
More information and booking |
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Technical Files and Design Dossiers for Medical Devices |
AMP Technology Centre, Sheffield |
01/May/2014
|
2 |
More information and booking |
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Quality System Product Realisation Process & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
19/May/2014
|
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
|
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
|
1/2 |
More information and booking |
|
Quality System Resource Management Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
20/May/2014
|
1/2 |
More information and booking |
|
Quality System CAPA & Improvement Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
21/May/2014
|
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
|
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 |
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Product Surveillance and Vigilance for Medical Devices |
AMP Technology Centre, Sheffield |
23/Jun/2014
|
1 |
More information and booking |
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Field Safety and Product Withdrawal for Medical Devices |
AMP Technology Centre, Sheffield |
24/Jun/2014
|
2 |
More information and booking |
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Post Market Surveillance for Medical Devices |
AMP Technology Centre, Sheffield |
26/Jun/2014
|
2 |
More information and booking |
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Structure of the Regulatory Agencies for Medical Devices |
AMP Technology Centre, Sheffield |
07/Jul/2014
|
1 |
More information and booking |
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Pre Market Technical Briefings for Medical Devices |
AMP Technology Centre, Sheffield |
08/Jul/2014
|
2 |
More information and booking |
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Regulatory Agency Enforcement & Remediation for Medical Devices |
AMP Technology Centre, Sheffield |
10/Jul/2014
|
2 |
More information and booking |
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Medical Device Research Methods |
AMP Technology Centre, Sheffield |
14/Jul/2014
|
1 |
More information and booking |
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Qualified Person Role & Responsibility for Medical Devices |
AMP Technology Centre, Sheffield |
15/Jul/2014
|
1 |
More information and booking |
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EU Medical Device CE Marking - Understanding |
AMP Technology Centre, Sheffield |
21/Jul/2014
|
1 |
More information and booking |
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EU Medical Device CE Marking - Implementing |
AMP Technology Centre, Sheffield |
22/Jul/2014
|
2 |
More information and booking |
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EU Medical Device CE Marking - Advanced |
AMP Technology Centre, Sheffield |
24/Jul/2014
|
2 |
More information and booking |
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Understanding Design Control for Medical Devices |
AMP Technology Centre, Sheffield |
18/Aug/2014
|
1 |
More information and booking |
|
Implementing Design Control for Medical Devices |
AMP Technology Centre, Sheffield |
19/Aug/2014
|
1 |
More information and booking |
|
Understanding Risk Management - ISO14971 for Medical Devices |
AMP Technology Centre, Sheffield |
20/Aug/2014
|
1 |
More information and booking |
|
Understanding Product Validation for Medical Devices |
AMP Technology Centre, Sheffield |
21/Aug/2014
|
1 |
More information and booking |
|
Planning and Conducting Clinical Investigations for Medical Devices |
AMP Technology Centre, Sheffield |
08/Sep/2014
|
1 |
More information and booking |
|
Medical Devices Clinical Evaluation – Step by Step |
AMP Technology Centre, Sheffield |
09/Sep/2014
|
2 |
More information and booking |
|
Post Market Clinical Follow up for Medical Devices |
AMP Technology Centre, Sheffield |
11/Sep/2014
|
2 |
More information and booking |
|
Medical Device Project Management |
AMP Technology Centre, Sheffield |
15/Sep/2014
|
1 |
More information and booking |
|
The Design History File for Medical Devices |
AMP Technology Centre, Sheffield |
29/Sep/2014
|
1 |
More information and booking |
|
Writing Technical Summaries for Medical Devices |
AMP Technology Centre, Sheffield |
30/Sep/2014
|
2 |
More information and booking |
|
Technical Files and Design Dossiers for Medical Devices |
AMP Technology Centre, Sheffield |
02/Oct/2014
|
2 |
More information and booking |
|
Quality System Product Realisation Process & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
20/Oct/2014
|
1/2 |
More information and booking |
|
ISO 13485 Quality System Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
20/Oct/2014
|
1/2 |
More information and booking |
|
Quality System Top Management Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
21/Oct/2014
|
1/2 |
More information and booking |
|
Quality System Resource Management Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
21/Oct/2014
|
1/2 |
More information and booking |
|
Quality System CAPA & Improvement Processes & Requirements for Medical Devices |
AMP Technology Centre, Sheffield |
22/Oct/2014
|
1/2 |
More information and booking |
|
Managing Suppliers within a Quality Management System Framework for Medical Devices |
AMP Technology Centre, Sheffield |
22/Oct/2014
|
1/2 |
More information and booking |
|
Medical Device Process Validation |
AMP Technology Centre, Sheffield |
23/Oct/2014
|
1 |
More information and booking |
|
Product Surveillance and Vigilance for Medical Devices |
AMP Technology Centre, Sheffield |
17/Nov/2014
|
1 |
More information and booking |
|
Field Safety and Product Withdrawal for Medical Devices |
AMP Technology Centre, Sheffield |
18/Nov/2014
|
2 |
More information and booking |
|
Post Market Surveillance for Medical Devices |
AMP Technology Centre, Sheffield |
20/Nov/2014
|
2 |
More information and booking |
|
Structure of the Regulatory Agencies for Medical Devices |
AMP Technology Centre, Sheffield |
01/Dec/2014
|
1 |
More information and booking |
|
Pre Market Technical Briefings for Medical Devices |
AMP Technology Centre, Sheffield |
02/Dec/2014
|
2 |
More information and booking |
|
Regulatory Agency Enforcement & Remediation for Medical Devices |
AMP Technology Centre, Sheffield |
04/Dec/2014
|
2 |
More information and booking |
|
Qualified Person Role & Responsibility for Medical Devices |
AMP Technology Centre, Sheffield |
08/Dec/2014
|
1 |
More information and booking |