Boyd Technologies has announced the certification of its quality management system to ISO 13485:2016.
ISO 13485:2016 is an internationally recognized quality standard to ensure the consistent design, development, production, installation, and sale of medical devices are safe for their intended purposes. To be certified, organizations must demonstrate an ability to provide medical devices and related services that consistently meet customer and regulatory requirements.
“Attaining our ISO 13485:2016 certification is a major milestone as it speaks to Boyd’s continuous focus on risk management and design control activities during product development and commercialization,” commented Dylan Spink, Director of Quality Assurance.
About Boyd Technologies
Boyd Technologies is an advanced materials and technology company operating in the medical device and life sciences market. The Company’s service platform provides material sourcing, product development, and advanced manufacturing services to global OEM partners in the medical and life sciences fields. Boyd Technologies is ISO 13485 certified and FDA registered as a contract manufacturer of medical devices. The Company has two locations, with headquarters and manufacturing in Lee, MA, and a sales and engineering office in Boston, MA. The Company was founded in 1979 and is privately held.