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This training provides participants with the understanding of the purpose and requirements of Directive 93/42/EEC, as amended by Directive 2007/47/EEC, in order to familiarize quality and regulatory professionals, engineers, supervisors and management with the technical documentation requirements.

Upon completion of this training delegates will be able to:

  • Understand the technical documentation requirements of Medical Device Directive 93/42/EEC
  • Prepare technical documentation to meet the requirements of the Medical Device Directive 93/42/EEC
  • Use the references and guidance documents available to further enhance their understanding of the documentation requirements

Contact SGS today for more information on SGS Technical Documentation for 93/42/EEC.