A QMS solution that fosters innovation.

Your Quality Management System (QMS) should support your organizational goals. By clarifying responsibilities and ensuring a structured flow of information, you are able to easily identify and minimize risk as your product moves from concept to manufacturing. We provide a compliant and proven electronic Quality Management System tailored to ISO 13485 and 21 CFR 820 and designed for efficiency.

ClearMark

Regulations and international standards are constantly changing and updating procedures takes time and attention.

Let ClearMark do that for you.

With the Regulatory Mark electronic Quality Management System, you get structured workflows for all aspects of your QMS, along with annual procedure updates to ensure that you will always be compliant. Our system is designed for compliance with ISO 13485 and 21 CFR 820 to make your FDA, ISO, or MDSAP audit run like clockwork.