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Patrícia da Silva Peres joins Qserve

Patrícia da Silva Peres

Qserve Group is pleased to announce that Patrícia da Silva Peres has joined our team to further expand its capabilities in supporting the medical device & IVD industries worldwide.

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.

About Qserve Group

Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.

Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our open job listings 

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