Dr Gerard Llimos

Dr Gerard Llimos

Project Associate

Dr Gerard Llimos is a biotechnologist by training and holds a Master’s in Systems Biology from the University of Luxembourg and the Roswell Park Cancer Institute. He also holds a PhD in Genetic Variations and Epigenetics from the Swiss Federal Institute of Technology in Lausanne (EPFL). Gerard has 6 years of experience in project design and management, data analysis and finally scientific writing and communication. At Medidee, Gerard supports you with the setup and review of the technical documentation for CE-marking, the strategy of clinical and performance evaluation for medical devices and in vitro diagnostic devices (IVDs), and, finally, with the setup and review of verification and validation activities particularly related to DNA sequencing, genetic engineering and digital health. Gerard is fluent in English, Spanish, Catalan and French.


Valentina Lintas - Medidee Services

Dr Valentina Lintas

Project Associate

Dr. Valentina Lintas is a biomedical engineer by education with a specialization in biomechanics and holds a PhD from the University of Zurich (UZH) with focus on tissue engineering applied to minimally invasive cardiovascular technologies. Before joining Medidee, she worked for a med-tech startup, gaining over 2 years of experience in Regulatory Affairs. Additionally, she completed a CAS CARAQA in Clinical Affairs, Regulatory and Quality for Medical Devices and In-Vitro Diagnostics. Valentina is eager to provide regulatory and quality support for compliance to European regulations, for the CE marking of medical devices and in vitro diagnostic devices. Valentina speaks fluently English and Italian.


Dr Cornelia List - Medidee Services

Dr Cornelia List

Senior Associate

Dr Cornelia List is a microbiologist by training with 5 years of research experience covering topics in genetics, environmental microbiology and infection biology. Her work has been presented at international conferences and published in peer-reviewed journals. Cornelia gathered her experience during her PhD (Swiss Federal Institute of Technology in Lausanne, EPFL) and during her Master’s study (University of Graz). She acquired experience in quality control in compliance with GMP requirements while working in the pharma industry, holds an apprenticeship as dental assistant and has been working for over 8 years with patients and dentists. Cornelia supports clients to assess the safety and performance of medical devices, including clinical evaluations and biological risk assessments. This includes the evaluation of biological risks to define a test plan and the evaluation of the results (toxicological risk assessment). Furthermore, she specializes in advising clients on additional requirements for substance-based medical devices. This implies the support in the establishment of classification and GSPR 12 documentation. Cornelia is fluent in German and English and has an intermediate level in French.


Elena Lucano - Medidee Services

Dr Elena Lucano

Training Manager & Senior Associate

Elena holds a PhD in Electronic Engineer from the University of Rome Sapienza. During her PhD, she carried out her research activities at the Division of Biomedical Physics at the U.S. Food and Drug Administration (FDA) laboratories (OSEL / CDRH).
She initially specialized in electromagnetic compatibility assessment of implantable medical devices with magnetic resonance imaging systems. The experience at the FDA laboratories exposed her to regulatory science oriented to Pre-Market research. She has a versatile experience on modeling and simulations, and conformity testing of medical devices to international standards.
At Medidee, Elena manages projects related to regulatory and quality compliance and is also in charge of the CARAQA training programs running in Yverdon-Les-Bains, Basel, Louvain-La-Neuve and Lübeck.
Elena speaks fluently Italian and English and has good understanding of French.


Eloïse Lovejoy - Medidee Services

Eloïse Lovejoy

Senior Consultant

Eloïse Lovejoy holds an HES Bachelor’s degree in Design and Materials and a Master of Science MSE in Industrial Technologies, with a specialization in the biomedical field. She has worked as regulatory associate for the implementation of the regulatory and quality control processes for a medical device intended for the Southern Hemisphere.
This background gives her a robust foundation and understanding of the operation of medical devices, as well as aspects connected to their development and production. Eloïse coaches QMS and product certification processes. Eloïse is also specialized in US requirements preparing FDA QSR audit.