Recovery Force ISO 13485 Certification

FOR IMMEDIATE RELEASE

ISO 13485, Medical devices – Quality Management Systems – requirements for regulatory purposes, is an internationally recognized standard for organizations involved in the medical device industry. Recovery Force’s quality system and controls are in place to design, manufacture, and distribute medical devices.  According to the International Organization for Standardization (ISO), which reviews standards every five years, the 2016 revision is a response to the “latest quality management system practices, including changes in technology and regulatory requirements and expectations.”

Facing regulatory hurdles and maintaining quality systems is a integral part of bringing a medical device to market. Ensuring safe use of products through requirements helps streamline and reinforce internal processes and procedures while carrying on with the changes and evolution affecting the market.

Recovery Force Quality Policy

“We are committed to the pursuit of excellence in the development and manufacturing of all Recovery Force products and will do this with the intent that each product could be used by one of our own family members. We are committed to compliance to regulatory requirements and the effective operation of the Quality System at Recovery Force.”