By outsourcing your medical device supplier audits to our quality control team, you can rest assured you’re making a wise cost-effective and time-saving decision.

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. 

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

First in Human refers to the phases of clinical research in which scientists conduct experiments with a health intervention to obtain sufficient evidence for a process considered effective as a medical treatment.

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

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.

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’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.