Allurmed was established in 2018 to provide professional regulatory and consulting services to the pharmaceutical, medical device and healthcare sectors. Since the beginning of our operations, our main objective has been to become a reliable and long-term partner for pharmaceutical manufacturers, medical device companies, distributors, importers and organisations involved in healthcare projects. Over the years, Allurmed has expanded its service portfolio and developed an integrated service model covering medicinal product registration, medical device registration, biologically active food product registration, pharmacovigilance, regulatory consulting and medical facility design. Our professional approach Allurmed’s work is not limited to the preparation and submission of documents. Each product and project is individually assessed from scientific, technical and regulatory perspectives. Our team identifies potential risks, detects documentation gaps and develops an appropriate regulatory strategy based on the client’s ob...