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 topics from IEC 60601-1 Third Edition to taking a closer look at the exporting of medical devices to various markets. More specifically, there are a number of trends happening across the medical device industry that one of our experts can answer. Is there a particular subject that your organization would like to learn more about? Or would you like to speak with one of our experts about one of the topics that this blog has covered in past months?
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. As the June 2012 deadline for Third Edition is quickly approaching, your organization might have a question for our expert. 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. Would you also like to know more about the exporting of medical devices and those requirements of other regions? 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.