Quality Standards & Certifications
ISO 13485 Certified for Medical Component Manufacturing
Springboard is ISO 13485 certified. “ISO 13485: Medical Devices—Quality Management Systems—Requirements for Regulatory Purposes” is an ISO standard that states the requirements for a comprehensive quality management system for the design/manufacture of medical components and sub-assemblies.
As stated on ISO.org, the ISO 13485 standard “specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical [components] and related services that consistently meet custom and applicable regulatory requirements. Such organizations can be involved in […] design and development, production, storage and distribution, installation, or servicing of a medical [component] and development or provision of [technical support]” or any combination of these processes.
Quality Standards for Your Unique Requirements
As needed, Springboard will work with you to develop a customized set of standards for your individual project. We can meet the quality demands of nearly any industry or application. Contact us to discuss your unique quality requirements.
Springboard: Quality You Can Depend On
No matter what your industry or application, the quality of your injection molded parts and products is our #1 priority. Request a quote today to get your project started, or contact Springboard to learn more about our quality standards and certifications.