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.
Per the EU Commission Recommendation of 9/24/2013 (2013/473/EU) Intertek is performing unannounced audits on its MDD clients for our MDD Notified Bodies, AMTAC and SEMKO.
The frequency and timing of unannounced inspections is decided by the Notified Body, but Intertek is required to perform at least one unannounced visit within a three year period. These audits are truly unannounced, and can occur at any location, including critical supplier premises, involved in the design, manufacture and support of CE marked medical devices.
Download this webinar to learn more about these mandatory unannounced audits from Intertek experts!