MedPro said its registration provides recognition that a company's processes are fully compliant with market expectations for quality medical device production and performance. The standard is known as ISO 13485, "Medical devices - Quality management systems - Requirements for regulatory purposes."
"This is not an easy designation to receive," said Craig Turner, MedPro CEO and Chairman. "It typically takes eighteen months to complete the process and we achieved it in seven. We are very pleased to have attained this certification, as it says a tremendous amount about MedPro, the quality of the products that we deliver, and the systems we have in place to ensure those standards are met. We believe this certification will instill added confidence in existing partners and open the door to develop current and future partnerships."
The International Organization for Standardization (ISO) is a worldwide federation of national standards bodies. ISO certification is an international standard that specifies a quality management system for the development, production and distribution of medical devices and related services.
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