The ClearMark implementation process includes three unique training sessions and customized quality planning to ensure a seamless transition of your Quality System. We believe in equipping our partners for success; training and service are provided with no hidden fees and at no extra cost to you. In addition to implementation and full-time customer support, every ClearMark client receives a full set of Standard Operating Procedures that have been compliance tested over time in both FDA and ISO 13485 audits.
If your team would like additional product specific regulatory support, we have a team of experts here to assist you. With over 100 years of experience in Regulatory and Quality affairs, our experts provide solutions that are practical and compliant. Whether your company is just entering the medical device market or you’re an established business in need of regulatory or quality support, our team knows what it takes to achieve your business goals.
More information on our services can be found at the consulting division of ClearMark, please visit us at regulatorymark.com.