Our company constitutes of people with high practical experience in EU regulatory affairs gained in Polish Authority and consulting companies. We are former Polish Authority experts who assessed dossiers in national procedure, MRP, DCP, central procedure (EMEA). We offer regulatory affairs services in EU: authorization of medicinal products, consulting on regulatory strategies, authorization of medical devices, food supplements, cosmetics, dossier auditing and preparation, PIL readability testing and other regulatory affairs services for pharma industry.