We take quality seriously, and hold ourselves to a rigorous standard in all that we do.
Catapult is committed to the development of safe and effective medical devices that consistently meet or exceed customer expectations. Our commitment to excellence is served through a robust Quality Management System (QMS) that is 21 CFR 820 FDA Quality System (QS) Regulation compliant and ISO 13485 Certified. Our certification is a testimony to Catapult’s commitment to providing the highest quality Design & Development services.
Catapult’s quality system allows for flexibility in our approach to each project. As an alternative to utilizing our internal quality system, Catapult can work within the client’s quality system when requested.
Need help setting up a new Quality Management System? Ask one of our specialists. We’ll customize a system that meets your current business needs and is scalable as you grow.
Already have a system but are strapped for resources? Let us know. We can help by performing and documenting your internal and/or supplier audits. We are here to help!