International Standards, Quality & Regulatory Compliance, Writing & Reviewing Technical Dossiers

"20+ years Combining Regulatory Science, Law and Business helping companies to comply with regulatory requirements"

BaysMartin Consulting provides premium regulatory affairs services. We create technical dossiers for FDA and Global submissions. We review and advise on scientific protocols and test reports. We are experts in successful execution and navigating through today's challenges in getting biotechnology products to market. The team has over 20 years of knowledge and experience in OTC drugs, IVDs, Medical Device, Cosmetics, and Pharmaceutical regulations including clinical and quality management systems.