Noremac consultants have extensive experience with assisting device manufacturers bring medical technology to the marketplace. From the 510 (k) submission to physician education regarding reimbursement for the device, Noremac provides a full scale list of services to meet the needs of our clients.

Our innovative consulting services combined with our extensive knowledge of reimbursement regulations ensure post-sale compliance and optimum reimbursement. Noremac has a long list of medical device companies who continue to utilize our services. Our services include but are not limited to: 510(k) submission, clinical trials, assistance with regulatory bodies, post-sale compliance, and patient advocacy. In addition, Noremac has created detailed procedures to support FDA trial sites with payer specifications such as insurance pre-authorization for the use of new technology and procedures. Noremac consultants have authored a multitude of coding and documentation manuals and handbooks for physicians and billing personnel. Noremac also offers assistance in educating payers through the creation of payer strategies and providing direction with high level payer disputes.

Noremac has years of experience with a variety of medical device products and technologies which has enabled us to develop innovative approaches to assist with all aspects of the medical device reimbursement process.