ISO-13485-blog

All posts by: Carlos Pereira da Cruz

Related Products
Integrated EU MDR & ISO 13485 Toolkit
All Policies, Procedures, and Records
Learn more
ISO 13485 Toolkit
All Policies, Procedures, and Records
Learn more
ISO 13485 Foundations course
Accredited Online Training by Top Experts
Enroll now
Upcoming free webinar
Advisera Kristina Zvonar Brkic
Presenter
Kristina Zvonar Brkic
Understanding the new European Medical Device Regulation and how ISO 13485 Supports it
Thursday – October 19, 2023
Register now
Suggested reading
What are the EU MDR technical documentation structure and requirements?
Advisera Kristina Zvonar Brkic Kristina Zvonar Brkic
April 6, 2021
...
read more
Managing medical device infrastructure requirements according to ISO 13485:2016
Advisera Waqas Imam Waqas Imam
June 28, 2017
The manufacturing, design, or supply of any product or service needs an infrastructure...
read more
How can ISO 13485 help with MDR compliance?
Advisera Kristina Zvonar Brkic Kristina Zvonar Brkic
March 9, 2020
As a medical device manufacturer, if you are implementing an ISO 13485:2016 Quality...
read more