Boyd Technologies Receives ISO 13485:2001 Certification

Boyd Technologies has announced the certification of its quality management system to ISO 13485:2001.

ISO 13485:2001 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 Stephen Boyd, CEO. 


About Boyd Biomedical

Boyd Biomedical is a growth partner for medical device and life sciences companies. Our growth platform provides a full suite of services to design, build, and launch regulated devices and liquid media solutions. We deliver innovation best to market.

The Company is ISO 13485 certified, and FDA registered as a contract design and manufacturing organization for medical devices. The Company has two locations: headquarters and manufacturing in Lee, Massachusetts, and a sales office in Boston, Massachusetts. The Company was founded in 1979 and is privately held. For more information about Boyd Biomedical, visit www.boydbiomedical.com.