Training Courses for Medical Devices

• ISO 13485 shapes quality management systems for medical device manufacturers all over the world
• We will explain how ISO 13485 is implemented and draw links with other quality standards

• This course is designed to provide you with knowledge and process steps to enable you to effectively implement a quality management system in accordance with the requirements of ISO 13485 certification.
• Don’t let standard slip-take the lead in maintaining Aerospace Quality Management Systems

• This course is intended for medical device quality professionals who are evaluating the effectiveness of the quality management system in their organization.
• This intensive course covers the principles and practices of effective quality management systems process audit in accordance with ISO 13485 and ISO 19011
• Our expert tutor will guide you through the internal audit processes from planning, reporting to corrective actions.

• This course covers the principles and practices of effective quality management in accordance with ISO 13485 and ISO 19011.”Guideline for Quality and/or Environmental Management Systems Auditing”.
• Our expert tutors will guide you through the entire audit process, from managing an audit programme to reporting on audit results.
• Participants will gain necessary auditing skills through a balance of formal classroom tutorial, practical role-playing, group workshops, and open forum discussion.

Learnning how to make informed decisions with regards to meeting the requirements of the EU Medical Devices Directives

Know how to identify the steps required to recuce the risks and uncertainty in the EU regulatory process and thus bring products to the EU market faster