OMC Medical Regulatory Consulting
OMC Medical offers regulatory services to MedTech clients starting from medical device design requirements according to the relevant applicable standards, obtaining relevant MoH certification or listings, establishing your devices in a new market, keep product licenses up to date until the product is End of Service (EOS). We specialize in Regulatory Affairs, supporting with global regulations (CE, FDA, UKCA, MedDo, CDSCO, NMPA), thereby saving the time spent on research and conflicting requirements. Visit us at www.omcmedical.com. OMC Medical are proud to partner with ABHI and are delighted to offer a free 30-minute consultation to ABHI members to answer their regulatory questions.
Please write to info@omcmedical.co.uk to take up this offer.