The accuracy of medical device translation is vital when translating labels or instructions for packaging of medical devices. They must comply with the EU's directives for medical devices and IVDs, and be understood by the reader to ensure the safety and performance of the device.
Our team of experts has developed a multi-stage workflow to eliminate risks in line with our certified quality procedures and standard operating procedures (SOPs).
RWS also offers verification, in-country review, certification and additional proofreading. Our workflows can also be adapted to suit your needs.
