August 30th, 2017:
If you are involved in the development of medical devices, it's likely you’ve heard the words design outputs. Well, “What are design outputs?” “What purpose do they serve?” and “Why should I be... read more
November 13th, 2017:
If you're in the market for a Human Factors Engineering (HFE) partner, our webinar explains the basics of HFE and regulatory affairs for combo-products and medical devices. Watch it today... read more
May 9th, 2019:
Why is ISO 13485 Certification Valuable for Medical Device Manufacturers? The medical device industry is one of the most highly regulated verticals worldwide. Devices and quality systems must... read more
Posted in: FDA
June 19th, 2019:
We are proud to announce Goddard has received ISO 13485:2016 certification! After more than 20 years of developing high-quality medical technology, we have taken our capabilities to the next level... read more
Posted in: FDA