Developing and managing proper quality guidelines for your medical devices and in vitro devices (IVDs) and any software as a medical device (SaMD) products is imperative. 

If you need help implementing, simplifying, or maintaining a quality management system for your medical device, in vitro device or pharmaceutical product, look no further than Cannon Quality Group. 

If you’re an entrepreneur in Medtech, IVD or software as a medical device (SaMD), you’ll want to set the stage for compliance early on, and Cannon Quality Group has a new cost-effective program to get you there.

At Cannon Quality Group, we have a reputation for right-sizing quality management systems to fit the product class, organization size, organizational stage, and business objectives.

Cannon Quality Group offers Food and Drug Branch compliance audits for certifications to medical device companies in California.

At Cannon Quality Group, we take a simple, risk-based approach to quality system regulation (QSR) compliance and FDA clearance.

Cannon Quality Group’s team of engineers are experts in the quality management field—they have the experience to grasp your project’s details immediately.

There’s a big difference between training delivered by a typical quality trainer and one delivered by a Cannon Quality Group quality management system professional. 

Our team can administar your Document Control Process and your eQMS process

Our team can perform as a Quality Engineering team member in your product development process

Our team can help you validate your production process, develop inspection plans, samples plans, perform guage R&Rs, execute Test method validations

Cannon Quality Group can help your company develop a valuable complaint management system that will help log, evaluate, and act on customer complaints quickly and purposefully, including assessing medical device reporting requirements.