Véronique Michel-Treil

Quality & Regulatory Affairs Director

Véronique is a clinical laboratory scientist, with more than 20 years’ experience in medical diagnostics and research laboratory settings. She led several hospital and private laboratories through successful quality accredi-tations. She held leadership roles in both Quality and Operations in an international Contract Research Organization (CRO), where she developed expertise in drug clinical trials and companion diagnostics (CDx). She led strategic development of molecular diag-nostic activities in 5 international sites located in Europe, USA, China and Asia-pa-cific. She oversaw innovative biomarker assays validation and implementation for diagnostics use in EU and US sites. Véronique focuses on regulatory and quality support for IVDs and clinical studies’ operation. She brings scientific expertise in Precision Medicine, Molecular Oncology, Phar-macogenomics, Infectious Diseases, Antimicrobial Resistance, and Immunoassays. Véronique speaks French and English.


Sara Morera Roca

Project Associate

Sara holds a Master’s in Biomedical Engineering from the University of Barcelona and the Polytechnical University of Catalonia. She has previously worked in various companies in design and engineering departments, where she gained experience in custom-made devices (prostheses and jigs) and serial production of implantable devices and single-use related instrumentation. She has experience working alongside surgeons and in usability engineering testing. Sara supports you in manufacturing process validation (IQ, OQ, PQ), preparation of technical documentation, management of suppliers and testing, and documentation for new product development. She has successfully conducted projects in the field of medical devices, such as technical file preparation for CE marking, risk management, QMS deployment and regulatory pathway analysis. Sara is fluent in English, Spanish and Catalan.


Dr Sergi Masgrau

Project Associate

Dr Sergi Masgrau is a biomedical scientist by training with an MSc in Biomolecules and Cellular Dynamics and a PhD in Medical Research in cardiovascular physiology and immunology. While conducting research at the Ludwig-Maximilians University of Munich, he gained expertise in various molecular biology and imaging techniques, alongside extensive experience in working with animal models. At Medidee, Sergi supports you in the review of the technical documentation for regulatory submission and in the related scientific aspects, such as the writing of clinical evaluations. He speaks fluently English, Spanish, German, and Catalan.


Dr Melina Maamir - Medidee

Melina Maamir, MD

Project Associate

Melina Maamir is a Medical Doctor with a passion for the medical device industry. She worked in the hospital as a general practitioner where she gained profound scientific knowledge and understanding of clinical needs. Melina holds a Master's Degree in International Healthcare Management from the International University of Berlin. Before joining Medidee, she worked in a medical device company where she performed medical writing work and redaction of clinical evaluation reports. At Medidee, Melina supports you with regulatory strategies, risk management, technical documentation and clinical aspects. Melina is fluent in French, English and Arabic.


Dr Neeru Mittal

Project Associate

Dr Neeru Mittal is a material scientist with expertise in design, synthesis, and characterization of materials for energy-related applications and has 9 years of research experience in nanotechnology, electrochemistry, analytical chemistry, and polymer chemistry. She obtained her integrated BS-MS degree, with a major in Chemistry from IISER-Mohali, India. Then, she moved from India to Switzerland to pursue her doctoral studies that focused on developing biodegradable batteries for green electronics at ETH Zurich. Over the course of her PhD study, she did an abroad stay in South Korea as a part of the Young Researchers’ Exchange Program, collaborated with scientists around the world, mentored 10+ undergraduate students, and published her research results in many peer-reviewed journals. She has gained extensive experience in scientific writing, project management, technical documentation and risk assessment while working in multiple international laboratories and start-ups. Neeru supports you in several medical device-related topics, such as the evaluation of biological safety of medical devices and the redaction of clinical evaluation reports. She is fluent in English and Hindi.


Dr Laia Morato - Medidee Services

Dr Laia Morató

Project Associate

Dr Laia Morató is a biologist by training and holds a MSc in neuroscience and a PhD in Biomedicine from the University of Barcelona. Laia continued her academic career as a postdoctoral fellow at the Swiss Federal Institute of Technology in Lausanne (EPFL). She has more than 10 years of professional experience in neuroscience and metabolic research, with a strong expertise in molecular biology and animal experimentation, and a solid understanding of diagnostic and therapeutic solutions for metabolic, neurodegenerative, and mental disorders. During her academic trajectory, she has also developed strong competencies in scientific writing, data and project management, as well as statistical analysis. Laia has published her work in prestigious peer-reviewed journals and presented at various international conferences. She is ready to support you with (pre-) clinical evaluations and review of technical documentation. Laia speaks fluently English, Spanish and Catalan and has a good understanding of French.


Medidee team member - Dr. Lydie Moreau

Dr Lydie Moreau

Project Associate

Dr Lydie Moreau is a biologist by training and holds a Ph.D. in food science and nutrition. She has a proven record of more than 15 years managing international projects in industry and academia. Lydie has experience in product development all the way from design to industrialisation. She then has successfully supported the research and development teams worldwide from a regulatory point of view to ensure compliance by design. This background gives her a solid understanding of the product development stages and the associated regulatory framework. Lydie has recently completed her Certificate of Advanced Studies for Regulatory, Quality and Clinical Affairs applied to medical devices. She is fluent in French and English.


Adrien Marchand - Medidee Services

Dr Adrien Marchand

Senior Associate

Dr. Marchand has 6 years of experience in research and development in the field of Bioanalytical Chemistry. Adrien holds a Master in Chemistry from the University or Liège and a PhD from the University of Bordeaux. He continued academic research as a Postdoctoral Fellow at ETH Zürich. Thanks to his PhD and Postdoctoral research, Adrien gained experience in bioanalytical chemistry and biophysics.
Adrien supports clients to assess the safety and performance of medical devices, including clinical and biological evaluations. This implies in particular the evaluation of the chemical and biological risks in order to define endpoints to be tested to safely place a product on the market, as well as the evaluation of the results, including toxicological risk assessment. Additionally, he defines regulatory strategies for medical devices and substance-based devices and supports cleaning and sterilization validations.
Adrien speaks fluently French and English.


Jarka Maierova - Medidee Services

Jarka Maierova

Finance & Administration

Jarka Maierova has 10+ years of experience in finance, accounting and administration in services and industrial companies. In Medidee, Jarka takes care of the compliance of business practices as well as of the delivery of services in Eastern Europe. Jarka masters German, Czech, English and Russian languages.


Michael Maier - Medidee Services

Michael Maier

Senior Partner

Michael Maier has 20+ years of hand on experience within medical device industry in design & development projects, product industrialization and regulatory & quality affairs. Michael is a trained Notified Body auditor for ISO 13485 and MDD with a broad scope of products. He has worked for the notified bodies of DEKRA and KEMA and covered international compliance programs as CMDCAS, J-PAL, TCP, TGA.
Michael combines sound technological knowledge with global regulatory expertise in medical devices. Michael holds an MBA in corporate management, a master in Medical Engineering and a Swiss Certificate of Capacity as precision mechanic. Regularly, he is speaker in international events for medical devices, quality and regulatory affairs topics.