Which standards are widely used by regulatory agencies to assess a company's ability to manufacture medical devices?

The correct answer highlights the use of ISO 13485 and ISO 14971, which are both critical standards recognized by regulatory agencies for evaluating a company's capabilities in manufacturing medical devices.

ISO 13485 specifically outlines the requirements for a quality management system (QMS) tailored to the medical device industry. This standard ensures that organizations consistently meet customer and regulatory requirements for the quality of medical devices. It emphasizes the need for a robust QMS that governs the entire life-cycle of a medical device, from design through production, installation, and servicing.

ISO 14971 complements this by providing a framework for risk management specifically for medical devices. It assists manufacturers in identifying, evaluating, controlling, and monitoring risks throughout the product's lifecycle, which is essential for ensuring the safety and effectiveness of medical devices.

Together, these standards form a comprehensive approach that regulatory agencies look for when assessing a manufacturer's compliance and ability to produce safe, effective, and high-quality medical devices.