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M5 - Global Quality System Requirements - ISO 13485 - Effective CAPA Investigations (QP) |
AMP Technology Centre, Sheffield |
20/Mar/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Planning for Content Deviations in ISO 14971:2012 (QP) |
Manchester - Venue to be confirmed |
13/Apr/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Understanding Design Control for Medical Devices (QP) |
Manchester - Venue to be confirmed |
13/Apr/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Implementing Design Control for Medical Devices (QP) |
Manchester - Venue to be confirmed |
14/Apr/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Understanding Risk Management – ISO 14971 for Medical Devices (QP) |
Manchester - Venue to be confirmed |
15/Apr/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Understanding Standards for CE Marking of Medical Devices (QP) |
Manchester - Venue to be confirmed |
16/Apr/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Risk Management for Software Based Medical Devices (QP) |
Manchester - Venue to be confirmed |
17/Apr/2015
|
1 |
More information and booking |
|
M6 - CE Post Market & Vigilance - Product Surveillance and Vigilance for CE Marking of Medical Devices (QP) |
London - Venue to be Confirmed |
20/Apr/2015
|
1 |
More information and booking |
|
M6 - CE Post Market & Vigilance - Field Safety and Recalls for CE Marked Medical Devices (QP) |
London - Venue to be Confirmed |
21/Apr/2015
|
2 |
More information and booking |
|
M6 - CE Post Market & Vigilance - Post Market Surveillance Plans for CE Marked Medical Devices (QP) |
London - Venue to be Confirmed |
23/Apr/2015
|
2 |
More information and booking |
|
M16 - Combination Product Requirements - Understanding Combination Product Regulations |
Manchester - Venue to be confirmed |
27/Apr/2015
|
1 |
More information and booking |
|
M16 - Combination Product Requirements - Combination Product Risk Management and Biological Evaluation – Key Issues |
Manchester - Venue to be confirmed |
28/Apr/2015
|
2 |
More information and booking |
|
M16 - Combination Product Requirements - Understanding the Safety and Usefulness of a Medicinal Substance for a Medical Device |
Manchester - Venue to be confirmed |
30/Apr/2015
|
1 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Advanced Audit Techniques |
Manchester - Venue to be confirmed |
05/May/2015
|
2 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Advanced Audit Techniques - Notified Body Auditing Techniques |
Manchester - Venue to be confirmed |
07/May/2015
|
1 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Medical Devices - Combination Products |
Manchester - Venue to be confirmed |
08/May/2015
|
1 |
More information and booking |
|
M7 - Working with Regulatory Agencies - Structure of the Regulatory Agencies for Medical Devices (QP) |
Manchester - Venue to be confirmed |
11/May/2015
|
1 |
More information and booking |
|
M9 - Biological Evaluation & Test Methods - EN ISO 10993: Biological Evaluation of Medical Devices (QP) |
AMP Technology Centre, Sheffield |
11/May/2015
|
1 |
More information and booking |
|
M7 - Working with Regulatory Agencies - Pre Market Technical Briefings for Medical Devices (QP) |
Manchester - Venue to be confirmed |
12/May/2015
|
2 |
More information and booking |
|
M9 - Biological Evaluation & Test Methods- Undertaking Biological Evaluation for CE Marking Step by Step (QP) |
AMP Technology Centre, Sheffield |
12/May/2015
|
2 |
More information and booking |
|
M7 - Working with Regulatory Agencies - Regulatory Agency Enforcement & Remediation for Medical Devices (QP) |
Manchester - Venue to be confirmed |
14/May/2015
|
2 |
More information and booking |
|
M9 - Biological Evaluation & Test Methods - Study Day Biological Evaluation and Product Safety for Complex M Technologies (QP) |
AMP Technology Centre, Sheffield |
14/May/2015
|
1 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Understanding and Preparing for the New EU Regulation (QP) |
Manchester - Venue to be confirmed |
18/May/2015
|
1 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Implementing (QP) |
Manchester - Venue to be confirmed |
19/May/2015
|
2 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Complex Borderline and Class III Medical Devices (QP) |
Manchester - Venue to be confirmed |
21/May/2015
|
1 |
More information and booking |
|
M17 - US Medical Device Regulations and Quality System Compliance Series |
AMP Technology Centre, Sheffield |
08/Jun/2015
|
4 |
More information and booking |
|
M4 - Pre & Post Market Technical File Data - The Design History File for Medical Devices (QP) |
Manchester - Venue to be confirmed |
12/Jun/2015
|
1 |
More information and booking |
|
M8 - The Professional Qualified Person - The Anticipated Role of the New Qualified Person for Medical Device CE Marking (QP) |
Manchester - Venue to be confirmed |
23/Jun/2015
|
1 |
More information and booking |
|
M8 - The Professional Qualified Person - Communicating Quality and Regulatory Strategy to Senior Leaders and Investors for Medical Device CE Marking (QP) |
Manchester - Venue to be confirmed |
24/Jun/2015
|
1 |
More information and booking |
|
M8 - The Professional Qualified Person - Project Management for Medical Devices – A Case Study Approach (QP) |
Manchester - Venue to be confirmed |
25/Jun/2015
|
1 |
More information and booking |
|
M13 - Process Validation Professional - Process Validation for Medical Devices – Planning and Conducting |
AMP Technology Centre, Sheffield |
07/Jul/2015
|
3 |
More information and booking |
|
M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software Regulatory Requirements - Step by Step |
AMP Technology Centre, Sheffield |
13/Jul/2015
|
1 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Planning and Conducting Clinical Investigations for Medical Devices |
AMP Technology Centre, Sheffield |
13/Jul/2015
|
1 |
More information and booking |
|
M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software - Technical File and Quality System Requirements |
AMP Technology Centre, Sheffield |
14/Jul/2015
|
2 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Medical Devices Clinical Evaluation - Step by Step (QP) |
AMP Technology Centre, Sheffield |
14/Jul/2015
|
2 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Post Market Clinical Follow Up for Medical Devices (QP) |
AMP Technology Centre, Sheffield |
16/Jul/2015
|
2 |
More information and booking |
|
M14 - Software Regulatory & Quality - CE Marking for Medical Devices Software Regulatory Requirements - Step by Step |
AMP Technology Centre, Sheffield |
16/Jul/2015
|
1 |
More information and booking |
|
M12 - Supplier Quality Professional - Understanding Supplier Control for Medical Devices – CE Marking |
AMP Technology Centre, Sheffield |
20/Jul/2015
|
1 |
More information and booking |
|
M12 - Supplier Quality Professional - Implementing Supplier Control for Medical Devices – CE Marking |
AMP Technology Centre, Sheffield |
21/Jul/2015
|
2 |
More information and booking |
|
M16 - Combination Product Requirements - Understanding Combination Product Regulations |
Manchester - Venue to be confirmed |
15/Sep/2015
|
1 |
More information and booking |
|
M16 - Combination Product Requirements - Combination Product Risk Management and Biological Evaluation – Key Issues |
Manchester - Venue to be confirmed |
16/Sep/2015
|
2 |
More information and booking |
|
M16 - Combination Product Requirements - Understanding the Safety and Usefulness of a Medicinal Substance for a Medical Device |
Manchester - Venue to be confirmed |
18/Sep/2015
|
1 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Understanding and Preparing for the New EU Regulation (QP) |
Manchester - Venue to be confirmed |
21/Sep/2015
|
1 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Implementing (QP) |
Manchester - Venue to be confirmed |
22/Sep/2015
|
2 |
More information and booking |
|
M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Complex Borderline and Class III Medical Devices (QP) |
Manchester - Venue to be confirmed |
24/Sep/2015
|
1 |
More information and booking |
|
M5 - Global Quality System Requirements - Introduction to ISO 13485 (QP) |
Manchester - Venue to be confirmed |
05/Oct/2015
|
1 |
More information and booking |
|
M5 - Global Quality System Requirements - Implementing ISO 13485 - A Project Management Approach (QP) |
Manchester - Venue to be confirmed |
06/Oct/2015
|
2 |
More information and booking |
|
M5 - Global Quality System Requirements - ISO 13485 Advanced - Effective Change Control (QP) |
Manchester - Venue to be confirmed |
08/Oct/2015
|
1 |
More information and booking |
|
M5 - Global Quality System Requirements - ISO 13485 Advanced - Effective CAPA Investigations (QP) |
Manchester - Venue to be confirmed |
09/Oct/2015
|
1 |
More information and booking |
|
M15 - IVD Regulations, Quality & Product Safety - Planning For the Revision of the IVD Directive 98/79/EEC |
Manchester - Venue to be confirmed |
19/Oct/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Implementing Design Control for Medical Devices (QP) |
Manchester - Venue to be confirmed |
19/Oct/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Understanding Risk Management – ISO 14971 for Medical Devices (QP) |
Manchester - Venue to be confirmed |
20/Oct/2015
|
1 |
More information and booking |
|
M15 - IVD Regulations, Quality & Product Safety - IVD CE Marking Regulatory Requirements – Step by Step |
Manchester - Venue to be confirmed |
20/Oct/2015
|
1 |
More information and booking |
|
M15 - IVD Regulations, Quality & Product Safety - IVD CE Marking Technical File Compilation & Management |
Manchester - Venue to be confirmed |
21/Oct/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Understanding Standards for CE Marking of Medical Devices (QP) |
Manchester - Venue to be confirmed |
21/Oct/2015
|
1 |
More information and booking |
|
M15 - IVD Regulations, Quality & Product Safety - IVD Clinical Data and Post Market Surveillance Plans |
Manchester - Venue to be confirmed |
22/Oct/2015
|
1 |
More information and booking |
|
M2 - Design, Risk and Safety Standards - Risk Management for Software Based Medical Devices (QP) |
Manchester - Venue to be confirmed |
23/Oct/2015
|
1 |
More information and booking |
|
M9 - Biological Evaluation & Test Methods - EN ISO 10993: Biological Evaluation of Medical Devices (QP) |
Manchester - Venue to be confirmed |
02/Nov/2015
|
1 |
More information and booking |
|
M9 - Biological Evaluation & Test Methods- Undertaking Biological Evaluation for CE Marking Step by Step (QP) |
Manchester - Venue to be confirmed |
03/Nov/2015
|
2 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Advanced Audit Techniques |
Manchester - Venue to be confirmed |
09/Nov/2015
|
2 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Advanced Audit Techniques - Notified Body Auditing Techniques |
Manchester - Venue to be confirmed |
11/Nov/2015
|
1 |
More information and booking |
|
M11 - Medical Device Auditing Professional - How to Audit Series - Medical Devices - Combination Products |
Manchester - Venue to be confirmed |
12/Nov/2015
|
1 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Planning and Conducting Clinical Investigations for Medical Devices |
Manchester - Venue to be confirmed |
23/Nov/2015
|
1 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Medical Devices Clinical Evaluation - Step by Step (QP) |
Manchester - Venue to be confirmed |
24/Nov/2015
|
2 |
More information and booking |
|
M3 - CE & Global Clinical Requirements - Post Market Clinical Follow Up for Medical Devices (QP) |
Manchester - Venue to be confirmed |
26/Nov/2015
|
2 |
More information and booking |
|
M17 - US Medical Device Regulations and Quality System Compliance Series |
AMP Technology Centre, Sheffield |
01/Dec/2015
|
4 |
More information and booking |
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