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Medical Devices Regulatory Training

Introductory Level CourseWriting Technical Files for Compliant Devices

 

Course overview

BSI’s Writing Technical Files for Compliant Devices one day course is designed to support manufactures by confirming current regulatory requirements of technical documentation.  The aim of the course is to speed the Notified Body certification process and enable manufacturers to sell compliant devices within the European Union.

On completion of training you will be able to identify and locate all regulatory requirements and guidance documentation necessary to write procedures enabling the creation and maintenance of compliant technical files and design dossiers.  

 

Course objectives and benefits

Learning Objectives

Upon completion of this training, delegates will be able to:

  • Confirm the technical documentation requirements as specified in the Directive
  • Interpret the general requirements of the Directive using relevant and harmonized standards together with various European & GHTF guidance documents for specific products
  • Define the process enabling the creation and maintenance of compliant technical files and design dossiers.
  • Explain the Notified Body certification process and level of response required to questions and nonconformities raised.

Benefits to your business

  • Generate technical documentation that support safe products that perform as intended meeting regulatory requirements – first time
  • Place products on the market in line with your critical launch dates
    Reduce costs by streamlining the certification process

 

 
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