Welcome to CiNQ systems, LLC – Now supporting the medical device, pharmaceutical and biologics manufacturing industries.

CiNQ systems supports healthcare product manufacturing industries through consulting, or as a contract resource. We understand Quality systems and assessing compliance with FDA 21 CFR Part 820, Parts 210 & 211, Part 58, ISO 13485 and ISO 9000.

CiNQ systems can implement complete quality systems to comply with these regulations and standards, and specifically excels in developing and implementing supplier controls systems, performing supplier evaluations and supplier audits. 

Size and location does matter, but not to us. We can support systems with a range in size and scope globally.

Most importantly, we deliver compliant systems that work with your business and its processes. Not just another canned system that provides limited flexibility and the future challenges of non-compliance.