Medical Writer, Biocompatibility
Patrícia started at Neodent, a subsidiary of Straumann AG, one of the leading device manufacturers in dental implants and accessories. Patrícia began as biological safety specialist, where she gained experience in biocompatibility, clinical evaluations and regulatory affairs. Her responsibilities were expanded to coordinate all biocompatibility studies and clinical evaluations for the company and get more involved in the regulatory process, design and development projects. She was also involved in audits and inspections from ANVISA, FDA, Notified Bodies and MDSAP audits and the transition from MDD to MDR.
Patrícia presents an impressive academic background combined with +5 years of experience in biological safety, toxicological analysis, systematic literature search and clinical evaluation (CEP/CER) in the medical device industry. Recently she was invited to be part of the Brazilian Committee discussing the CD-2 of the new ISO 10993-17. Her expertise is in the Dentistry field, including the analysis of dental implants, aligners, prosthetic abutments, instruments and resins. With Patrícia’s scope of work, she will move into Qserve’s new business unit Clinical Operations. While an important part of her work relates to medical writing, she will help our clients on biocompatibility projects as well.
She holds a PhD, Biochemistry & MSc, Biochemistry from Federal University of Paraná (UFPR), Curitiba/Brazil. Patrícia also holds a Bachelor in Mechanical Engineering from UFPR and a Bachelor in Biomedical Sciences from the State University of Londrina (UEL), Londrina/Brazil.
Learn more about Qserve CRO