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Establishing Compliance with the Medical Device Directive 93/42/EEC (MDD)

Reference Number: 511 Dates :2nd - 4th December 2008 Venue : London UK
Send me an email about the next course as I cannot make this date and/or location
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Summary | For whom intended | Objectives | Topics | Pre-requisites | Registration |

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
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  • 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

If this training course is not currently scheduled for a public presentation, then the next date is dependant upon demand. If you wish to be kept informed of future scheduling for this course please submit the form below with your complete details. Thank you.

Alternatively to run this or a similar course as an "In-house" course, or make any other enquiry please fill in your details and submit the form below. Please include either the course reference number or title.- Thank you.
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