Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Over the last few months, this blog has featured various experts that specialize in the medical device market. More specifically, these experts have deep knowledge spanning technical knowledge to providing counsel to customers on a variety of topics within this industry.
One expert who is frequently featured and can provide insight and technical insight into the IEC 60601-1 Third Edition is Todd Konieczny, North American Medical Technical Leader. In the coming weeks, Todd will further look at creep age and clearance requirements, among other topics. To ask Todd a question or to further speak with him about your upcoming project, please send an e-mail to ThirdEdition@intertek.com.
Additionally, this blog looks at the Medical Device Directive requirements and ISO 14971. The expert who can best address the questions and comments for these two topics is Christine Forcier, Program Manager for the medical device sector at Intertek. To ask Christine a question or to further speak with her about your upcoming project, please send an e-mail to firstname.lastname@example.org.
To learn more and or to speak with an Intertek expert on this subject matter, please visit www.intertek.com/medical.