What is the main purpose of a "Technical File" in device regulation?

The main purpose of a "Technical File" in device regulation is to demonstrate compliance with regulatory requirements, particularly for CE marking in the European Union. This document serves as evidence that a medical device meets the necessary safety and performance standards as set out in EU legislation, such as the Medical Device Regulation (MDR) or the In Vitro Diagnostic Regulation (IVDR). A Technical File typically includes detailed information about the device, such as design specifications, risk assessments, testing data, manufacturing processes, and quality management systems.

This comprehensive documentation enables notified bodies and regulatory authorities to evaluate whether the device conforms to applicable directives, ensuring that it is safe for its intended use before it can be marketed in the EU. The emphasis on regulatory compliance is critical for manufacturers to obtain the necessary approvals and to maintain market access.

In contrast, the other options focus on aspects unrelated to regulatory compliance. Advertising features and pricing, publishing reviews, or outlining production costs do not contribute to establishing compliance with the necessary regulatory framework, which is the primary goal of the Technical File.