Exhibitors & Products at MEDICA & COMPAMED

Develop MDR-compliant medical devices smoothly and efficiently Get a well-coordinated team from medical technology, regulatory affairs and management on board.   What challenges have you faced

About Us Providing expertise in bioanalysis and logistics 0   As experts in biomarkers, bioanalysis, pharmacokinetics, logistics and quality systems management A4P deliver scientifically robust,

Achilles Design is a design research and development company that supports clients in translating their ideas into successful products, services and brands. Our multidisciplinary team of designers,

GDPR24/Privacy24 provides virtual data protection officers as required by GDPr and other data privacy regulations throughout the world. in addition to the vDPO services, we offer consulting

Andaman Medical is a regulatory affairs and market access consultancy specializing in the registration, authorized representation, importation and master distribution of medical devices and in-vitro

ARQon Group expanded from Regulatory consultancy to Commercial advisory, Training and Digital platform to help companies to gain global market access. Our Portfolios includes Global registration,

BCI Global carries out research, advises, implements and performs project management in the areas of supply chain strategy and design, international business strategy, location search and site

At the German government's stand at the MEDICA medical technology trade fair in Düsseldorf from November 14 to 17, 2022, they can find out what requirements medical device manufacturers have to

Clinical Consulting -  full service CRO in Poland. Regulatory affairs and clinical operations partner in product development, laboratory analytics and QP certification. We are working with

DeSia was founded by Pınar NEBOL who has deep experience over 10 years in Medical Device Clinical Affairs. Our goal as a consulting& CR company is to provide a wide range of

I'm a global Quality Assurance and Regulatory Affairs specialist with over twenty three years’ experience in the Medical Devices & IVD sectors. Accredited as an Internationally Certified

Based on a solid experience, the FSE GROUP has over the years become one of the leading companies implementing biomedical and laboratory equipment projects in international markets. Since we have

GiDoS SPRL is a quality-driven, service-oriented regulatory affairs company, located in Brussels, Belgium. Our main service area is in the medical sector, focusing on Medical Devices and In-Vitro