An NSF International Company M8 - The Professional Qualified Person - The Anticipated Role of the New Qualified Person for Medical Device CE Marking (QP)
PrintPart of Medical Devices QP Training Module 8
£735.00 exl VAT
About this course
A one day course providing you with the necessary overview as to the anticipated role of the Qualified Person. We go beyond the basic requirement in Article 13 of the draft European Medical Device Regulation and take you through the practical realities about being responsible for medical devices at the specification development, manufacture, release, distribution and authorized representative areas. We outline the critical decisions you make, the specific competencies you require and drive home the practical experience and education expectations that will ensure you have the right people in the right place. We do not make claims about the similarity of the QP in pharma, instead we concentrate upon the very real issue of ensuring that the people managing regulatory compliance in medical devices are confident in their competence.
Who Should Attend
The module is aimed at quality and regulatory professionals wishing to build upon their technical skills and move into formal career development by discussing project management, management and presentation behaviors.
