There is no need to worry when taking the step towards a quality management system according to EN ISO 13485 for medical device manufacturers.
Since the MDR we are also affected by the mandatory QM system in Class I. Take advantage of the opportunity to discuss your needs with us at our stand at REHACARE Hall 04 / Booth E03, how we can work together to get your company off the ground or continue along a path you have already started, because one thing is clear: a QM system must be well planned and structured so that it is not an obstacle in day-to-day business but rather a help for your company.
This discussion will enable you to better understand EN ISO 13485 and use it meaningfully for your organisations quality management system. In doing so, we take over established and proven methods where it makes sense to do so, and create new ones where it is helpful.
This discussion will enable you to better understand EN ISO 13485 and use it meaningfully for your organisation. Feel free to contact us – we are here to advise and support you.
(1 Rating(s), average: 5.00 out of 5)
Loading...
