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FDA and DIN ISO Standards

pro med instruments is committed to providing quality products, continuous product and process improvements and excellent customer satisfaction. A Quality Management System has been implemented throughout the company covering all relevant standards.

The company and the products we manufacture follow the Good Manufacturing Process (GMP) of the Food and Drug Administration (FDA), ISO Standards and other relevant standards. Beyond that, additional country-specific registrations exist for various markets.

This is understood to be a guarantee that pro med instruments manufactures, supports and services the DORO® product line in compliance with precise documented quality policies and procedures.

In our endeavor to continuously improve and refine our processes, we have the efficiency of these processes and management systems regularly verified and certified by governing bodies.