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Establishing Compliance with the Medical Device Directive 93/42/EEC (MDD) |
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| Summary | For whom intended | Objectives | Topics | Pre-requisites | Registration | |
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Training Course Summary
This three day training course covers the content of the Directive in some detail
and the intention is to assist delegates in becoming
familiar with its provisions. All key aspects are
addressed, enabling participants to navigate between
the Articles and Annexes with confidence. It is
designed to be of assistance to personnel within
quality assurance and regulatory affairs departments,
and to staff within Notified Bodies and Competent
Authorities who are expected to audit against the
Directive or to administer its provisions. |
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Objectives
In the context of compliance with the MDD (93/42/EEC) to understand:
- The role of European Directives
- Legal necessity for compliance
- The structure of the Directive
- The mechanisms of compliance
- The importance of the concept of risk
- How to find the key elements within the text of the Directive
- The roles of the various functions within the organization including those at all levels
of management
- The role of external bodies such as Notified Bodies and Competent Authorities
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For whom intended
Anyone within the company’s management structure
whose role is impacted by the requirement for the
organization to comply with the MDD or
EN ISO 13485:2003 but in particular:
- Quality assurance personnel
- Regulatory affairs personnel
- Notified Body auditors
- Competent Authority personnel involved in the enforcement of the Directive
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Pre-requisites
Delegates will be expected to have educational levels appropriate to the functions listed above. Some
familiarity with the MDD and EN ISO 13485:2003 would be an advantage but is not a requirement. |
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Topics covered include:
- Background to European Regulation of Medical
Devices (MDD)
- Development of European Directives
- Common steps to compliance
- Product classification
- Technical documentation
- Role of Competent Authority, Notified Body and Manufacture
- Role of harmonized standards including ISO 13485:2003
- Conformity assessment routes
- Technical documentation (technical files)
- ‘Private Labelling’
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Further Information
- Date : The next Public presentation is 2nd - 4th December 2008
- Price : £995.00 + VAT
- Venue : London, UK
- Registration: To register please fill in your details on the form below and submit it - Thank you
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