ISO 13485: What You Need to Know to Build a Quality Management Systems for Medical Devices

In this video, we discuss the key documents required to build a quality management system (QMS) for medical devices and how to comply with ISO 13485. We explain the purpose and importance of each document, and provide practical tips on how to successfully implement a QMS. Whether you're a startup or an established company, this video will help you build a robust QMS to ensure compliance with regulatory requirements and deliver safe and effective medical devices to the market.
Contact us for ISO13485 Services - www.zimmerpeacock.com/contact/
ISO13485 Services - www.zimmerpeacock.com/quality/

[@michelimuzie3977]

I loved the way you use your slides. What kind of program is that very well done video! Thank you for sharing it!

[@zimmerpeacock9703]

Thank you, the engineer who made this is a very diligent person :)

[@carlonemeno5600]

Hello! I have a question of you don't mind. If a medical device manufacturer is ISO 13485 certified as part of the MDR requirements, does that mean that all the company's products should adhere to its QMS? Or only those products that are considered as medical devices? In other words, do the non-medical device products of the company also need to adhere to its company's QMS?

[@zimmerpeacock9703]

Good question. Please post your question here and we will cover it in a future webinar - www.zimmerpeacock.com/contact/