Medical devices must comply with numerous rigorous standards and regulations to access the market and, ultimately, improve patient treatment.
From the EU’s Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) to key ISO standards like ISO 13485 (medical devices quality management systems), we have a range of courses to suit your needs.
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Why SGS?
We are the world’s leading testing, inspection and certification company, recognized as the global benchmark for sustainability, quality and integrity. Wherever you are, whatever your industry, our experts worldwide provide specialized solutions to make your business faster, simpler and more efficient. With in-depth expertise in medical device standards, we can help you understand the requirements and support your certification path.
To discuss your medical devices training requirements, contact us today.