ASPHALION
Talyta Carteano is an experienced professional in the medical devices field, currently serving as the Medical Devices Director at ASPHALION since September 2020, where responsibilities include managing certification processes and project timelines. Previous roles include Head of Quality and Regulatory Affairs at QMENTA Inc, focusing on quality management systems and audit programs, and Regulatory Affairs Director at Devicare, overseeing regulatory compliance and product registration in EMEA and LATAM. Talyta's earlier experience includes project management and engineering roles at Micromar, contributing to the design and development of medical devices. Talyta holds a Master's degree in Biomedical Engineering from Universitat de Barcelona and a Bachelor of Engineering in Mechanical Engineering from Universidade do Grande ABC.
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ASPHALION
ASPHALION is an International Scientific and Regulatory Affairs consultancy firm based in Barcelona and Munich.They offer comprehensive services for Drug Development and Regulatory Affairs to Pharma, Biotech and Medical Devices companies.Since 2000, we have consistently grown and now have over 70 professional consultants with backgrounds inLife sciences (Pharmacy, Chemistry, Biology, Biochemistry, Biotechnology, Medicine and Veterinary Medicine). Their consultants are experts in their field and are in direct contact with EU agencies (EMA and NCAs) for the development and implementation of new regulatory standards.Asphalion provides a global range of services, for global clients. Their services range from early development, throughout the registration, until marketing and post-commercialization phases of your product.