Regulatory Affairs

Local regulatory experts for Pharma, Biotech and Medical Device companies across Europe, CIS/EAEU, and MENA regions from dossier development to full life-cycle management. Our full range of regulatory affairs solutions and services are dedicated to delivering the highest quality support, assistance and regulatory approvals. We follow the needs of our customer and their portfolios, as we work with a wide range of product categories: medicinal products, medical devices, cosmetics, and food supplements. Our Regulatory Affairs team has comprehensive expertise and assures quality and accuracy for each task. All team members have majored in life sciences.

Riaantech expertise ranges from developing and executing your regulatory strategy to pave the way for Marketing Approval. By combining our in-house regulatory expertise with scientific know-how, we help you to ask the right questions and to keep the end goal in mind during early development. Our focus is on enabling you to navigate the landscape of complicated regulations and compliance hurdles and provide you with a clear strategy for successful commercialization. In addition to complicated regulations and compliance hurdles, we also deliver specific support concerning local needs as they are fundamental to any strategic regulatory decision. As an extension of your team, we cooperate with you every step of the way towards Marketing Authorization.