EU, US, Japan, Korea, Brazil.
MD101 was founded to assist medical device companies in developing and bringing products to market, accelerating time-to-market, and ensuring compliance with regulatory standards.
With its large network of experts, MD101 provides mastery in a myriad of medical devices and is equipped to handle whatever challenge a manufacturer is facing, whether it is quality assurance, regulatory affairs, clinical affairs, reimbursement strategy, or international business development.
At MD101, we bring you the power of our unique value proposition, focused on healthcare, and the experience of a team that will ensure your business’s success.
Areas of regulatory/reimbursement support:
Quality Assurance – Regulatory Affairs (CE, FDA) – Software Medical Devices standards – Clinical Strategy – Reimbursement Strategy and Dossier – Value Dossier.