GemarMed srl

GemarMed srl stands as a premier legislative office, offering friendly and pragmatic advice to the medical device and pharmaceutical industries, particularly in GXP, Quality, and Regulatory Affairs. With a rich history dating back to its establishment in 2004, GemarMed is dedicated to providing unparalleled expertise and support to companies navigating the complex landscape of medical technology regulations.

Located in Medolla, Modena, at Via G. Amendola, 43 and Via G. Puccini, 1, GemarMed srl boasts a team of seasoned professionals, including experienced quality system and GMP auditors, clinical study personnel, regulatory affairs specialists, engineers, and computer system validation experts. This comprehensive team allows GemarMed to offer pragmatic solutions that help clients achieve both their regulatory and business objectives.

GemarMed srl specializes in process validation, United States Agent Services, Canadian Regulatory Requirements, U.S. Pre-Market Approvals, CE Marking, and more. GemarMed is committed to delivering the highest level of expert advice and hands-on assistance in complying with US and European regulatory, quality system, GMP, and clinical data requirements. We invite the management of GemarMed srl to create a customized and exclusive company showcase and product listing on our platform to further enhance your market presence.