{"id":12035,"date":"2025-09-22T17:18:10","date_gmt":"2025-09-22T17:18:10","guid":{"rendered":"https:\/\/mdxcro.com\/a-propos\/notre-equipe\/"},"modified":"2026-07-22T10:15:16","modified_gmt":"2026-07-22T10:15:16","slug":"equipe","status":"publish","type":"page","link":"https:\/\/mdxcro.com\/fr\/qui-sommes-nous\/equipe\/","title":{"rendered":"Notre \u00e9quipe"},"content":{"rendered":"\n
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Rencontrez les experts qui garantissent la r\u00e9ussite r\u00e9glementaire et clinique<\/h1>\n \n

Notre \u00e9quipe fait la diff\u00e9rence chez MDx \u2014 un r\u00e9seau diversifi\u00e9 de professionnels chevronn\u00e9s, d’anciens experts d’organismes notifi\u00e9s, de chercheurs cliniques, de responsables AQ, de scientifiques titulaires d’un doctorat et d’innovateurs en technologies m\u00e9dicales qui collaborent pour garantir l’excellence \u00e0 chaque \u00e9tape du cycle de vie du produit.<\/span><\/p>\n<\/div>\n \n <\/div>\n <\/div>\n<\/section>\n\n

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\n \n
\n
\n \"David\n \n \n
\n Leadership <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical research leader and MedTech entrepreneur with deep expertise in medical devices, IVDs & precision medicine, with global study experience. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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David Tom\u00e9<\/h3>\n

President<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Carlos\n \n \n
\n Leadership <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Senior regulatory leader and former BSI IVDR reviewer with deep experience in CE marking high-risk IVDs, companion diagnostics, and IVDR implementation. <\/div>\n <\/div>\n <\/div>\n\n \n
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\n

Carlos Galamba<\/h3>\n

CEO<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
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\n \"Alberto\n \n \n
\n Leadership <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Senior med-tech expert & ex-Notified Body reviewer with deep experience in high-risk implants, orthopedics, dental & neurology. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Alberto Bardaj\u00ed<\/h3>\n

Head of Medical Devices<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Clara\n \n \n
\n Leadership <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Strategic executive with nearly two decades of leadership experience in global talent acquisition, strategic resourcing, and business operations within the clinical research industry. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Clara Veldman<\/h3>\n

Head of Business Development<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
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\n \"Kirsty\n \n \n
\n Leadership <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Clinical Operations leader with IVD and CDx device expertise, delivering global clinical studies while establishing best practices and high performing teams. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Kirsty Macleod<\/h3>\n

Head of Clinical Research<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Catarina\n \n \n
\n Leadership <\/div>\n
\n EU <\/div>\n\n \n
\n
\n IVD Director at MDxCRO with over 5 years of experience in the diagnostics and in vitro diagnostics space. Specializing in IVDR regulatory strategy, Catarina supports MedTech and diagnostics companies in navigating the evolving European regulatory landscape. <\/div>\n <\/div>\n <\/div>\n\n \n
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Catarina Sep\u00falveda PhD.<\/h3>\n

IVD Director<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
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\n \"Andreia\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n PhD in Systems Biology, a Master\u2019s degree in Biotechnology and Cell Biology, and a degree in Biology, with training rooted in molecular genetics, cell biology, and translational biomedical research. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Andreia Henriques Ph.D.<\/h3>\n

Regulatory Affairs Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
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\n \"Alice\n \n \n
\n Regulatory <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Quality & Regulatory Affairs leader with global IVD expertise, guiding products to compliance across EU IVDR, FDA & beyond. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Alice Toomey-Smith<\/h3>\n

Regulatory Director, IVD<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Luis\n \n \n
\n Operations <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Luis is an IT and cybersecurity professional with 8+ years\u2019 experience in cloud, compliance, governance, and leading multidisciplinary teams. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Luis Pereira<\/h3>\n

IT Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Joana\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
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\n Molecular genetics and biomedical sciences professional with over seven years\u2019 experience in NGS workflows, quality assessment, and cancer therapeutics research. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Joana Silva<\/h3>\n

Regulatory Affairs Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Yaiza\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
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\n Senior Clinical Research Manager and biomedical engineer, expert in study design and clinical operations, MDR\/IVDR regulatory compliance, GCP, CDx, and precision medicine. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Yaiza Benito<\/h3>\n

Clinical Research Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Bego\u00f1a\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Lead in medtech, with expertise in CDx, MDR\/IVDR, FDA\/EMA and clinical operations management. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Bego\u00f1a Fernandez<\/h3>\n

Clinical Research Lead<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Catarina\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Specialist in oncology and radiation therapy clinical activities, clinical research manager with broad experience across medical devices and clinical operations. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Catarina Pragana<\/h3>\n

Senior Manager Clinical Operations<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Virginia\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Principal RA Consultant IVD, life sciences academic background with a Biochemistry degree by Universidade do Porto and a PhD in Molecular Biosciences by Universidad Auton\u00f3ma de Madrid. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Virginia Gondar, PhD.<\/h3>\n

Principal RA Consultant IVD<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Antonino\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Specialist with cardiovascular CRC MedTech experience and healthcare background, focusing on CRA. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Antonino Barbera<\/h3>\n

Clinical Research Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Ana\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Ana Sofia Silva joins MDx as a Clinical Research Specialist, bringing a strong scientific background and hands\u2011on experience in clinical operations across Europe. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Ana Sofia Silva, PhD.<\/h3>\n

Clinical Research Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Katharina\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Pro, expertise in IVDR\/MDR & ISO, leading trials in medical devices, IVDs & companion diagnostics across regions <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Katharina Peters, PhD<\/h3>\n

Associate Director Clinical Affairs<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Marketa\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Expert in Precision Medicine, NGS & CDx, combining technical and regulatory expertise to guide IVDs through CE certification and clinical trials, ensuring compliance with EU IVDR. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Marketa Svobodova, PhD<\/h3>\n

Regulatory Director, Precision Medicine<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Andre\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Senior quality & regulatory expert, ISO 13485\/MDR\/IVDR auditor with expertise in CE marking MDs\/IVDs, incl. dental, implantables, drug delivery, genomic tests, & MDR\/IVDR implementation. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Andre Moreira<\/h3>\n

Regulatory Director, Medtech<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Achille\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n With more than 7 years of experience as Human Factors engineer, Achille Gautheron is interested in the evolution of medical devices and In-Vitro Diagnostic Devices to improve patient well-being and care provided by practitioners. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Achille Gautheron<\/h3>\n

Sr. Human Factors Engineer<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Human Factors Engineer with an R&D background across medical devices and IVD, focused on building technologies that fit real clinical workflows and patient use. <\/div>\n <\/div>\n <\/div>\n\n \n
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\n

Paula Galan<\/h3>\n

Human Factors Engineer<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Xabier\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Senior RA\/QA consultant with Post-Market Surveillance, Clinical evaluation, Risk Management and Human Factor Engineering expertise supporting Medical Devices & IVDs <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Xabier Arias, PhD<\/h3>\n

Senior RA\/QA consultant <\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Huiwen\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical research lead with expertise as a CRA and submission specialist across MD, IVD, and drug studies. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Huiwen Xu, PhD<\/h3>\n

Clinical Research Lead<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Victoria\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Medtech Manager with RA, QA & CRA experience (FDA, UK, MDR\/IVDR, TGA), specialized in clinical evidence, IVF & drug\u2013device combination products. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Victoria Bachiller<\/h3>\n

Medtech Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Helen\n \n \n
\n Clinical <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Clinical Research Lead in IVDs and CDx, clinical affairs, operations, and EU\/UK data protection compliance. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Helen Chen<\/h3>\n

Clinical Research Lead<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Nicholas\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Global medtech expert with 20y in IVD\/MD, regulatory consulting & clinical research across AUS, UK, EU, UAE & Switzerland. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Nicholas Wilson, PhD<\/h3>\n

Principal RA Consultant<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Patricia\n \n \n
\n Operations <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Healthcare professional with CDx & IVD experience, combining commercial, administrative, and management expertise with strong team leadership. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Patricia Fernandes<\/h3>\n

EA & BO Coordinator<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Claudia\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Regulatory affairs specialist with extensive experience in IVDR implementation, precision medicine, and software regulation, backed by hands-on laboratory and R&D experience in various biological disciplines. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Claudia Loureiro, PhD<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Ana\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Specialist with strong scientific background in clinical microbiology and expertise in regulatory compliance with ISO 13485 and IVDR. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Ana Dias, PhD<\/h3>\n

Clinical Research Specialist <\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Pedro\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Specialist in Quality Management Systems and Molecular Biology, applying NGS Technologies to advance Precision Medicine. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Pedro Penedo<\/h3>\n

QARA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Floella\n \n \n
\n Regulatory <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Senior QA\/RA consultant with MDR, IVDR, Usability\/Human Factors and MDSW expertise, supporting MedTech and IVD innovation globally. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Floella Otudeko<\/h3>\n

Senior QARA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Marta\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Lead in IVDs, CDx, and medical devices. Skilled in performance study submissions and clinical operations under IVDR\/MDR, with focus on precision medicine and EU regulatory alignment. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Marta Crespo<\/h3>\n

Clinical Research Lead<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"F\u00e1tima\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical research specialist (PhD) with expertise in oncology, regeneration, pathology; skilled in IVDR CDx EU submissions and MDR CEVs. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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F\u00e1tima Manzano, PhD<\/h3>\n

Clinical Research Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
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\n \"Carmen\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research & Biostatistician Intern trained in biotech and biostatistics, supporting data-driven medtech clinical studies. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Carmen M\u00e9ndez S\u00e1nchez<\/h3>\n

Clinical Research Strategist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Miriam\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Regulatory Affairs Specialist in Precision Medicine with expertise in IVDR, NGS diagnostics, and clinical evidence generation. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Miriam Jauset, PhD<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Joana\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Joana has a background in genomics and molecular diagnostics, with a focus on next-generation sequencing (NGS) and precision medicine <\/div>\n <\/div>\n <\/div>\n\n \n
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\n

Joana Guerra, PhD<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Petrina\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Specialist\/CRA in MedTech & IVD; MDR\/IVDR, ISO 14155\/20916, clinical monitoring & regulatory submissions. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Petrina Mosoroceanu<\/h3>\n

Clinical Research Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Joana\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Quality & Regulatory Assurance Specialist with expertise in MDR compliance, QMS, audits, and medical device documentation. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Joana Santos<\/h3>\n

QARA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"Lucia\n \n \n
\n Operations <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Marketing Manager with with a background in industrial design, strong focus on digital business strategy and sustainable growth. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
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Lucia Pallas<\/h3>\n

Marketing Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Regulatory Affairs & PRRC professional specialized in IVDR, bridging molecular biology expertise with regulatory and quality frameworks. <\/div>\n <\/div>\n <\/div>\n\n \n
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In\u00e9s Eul\u00e1lio<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

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\n \n
\n
\n \"\u00c1lvaro\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical operations expert with focus on regulatory compliance and study set-up and oversight under ISO 14155 \/ 20916 and MDR \/ IVDR \/ FDA. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

\u00c1lvaro Torcal<\/h3>\n

Clinical Research Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Sonia\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Lead & Biostatistician with 4+ years in pharma and medtech trials across EU and US, MDR & IVDR, and ISO 14155 & 20916. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Sonia Ferreira, PhD<\/h3>\n

Clinical Research Lead & Biostatistician<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Miguel\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Clinical Research Strategist with a biotech background and clinical research training, focused on clinical operations within MDR\/IVDR frameworks. <\/div>\n <\/div>\n <\/div>\n\n \n
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\n

Miguel Lucas<\/h3>\n

Clinical Research Strategist <\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \n \n
\n Operations <\/div>\n
\n EU <\/div>\n\n \n
\n
\n A medtech professional with a biomedical engineering background, regulatory expertise (ISO 13485,MDR), and commercial operations experience. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Joana Figueiredo<\/h3>\n

Finance and Administration Coordinator (Purchases Representative)<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Emma\n \n \n
\n Regulatory <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Senior Medtech regulatory professional experienced in MDR and IVDR implementation, CE-marking high-risk devices, and FDA compliance. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Emma Cartwright<\/h3>\n

Senior RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Monica\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n IVD Quality and Regulatory Specialist with expertise in IVDR, ISO 13485, CE marking & molecular diagnostics tests. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Monica Rodrigues, PhD<\/h3>\n

QARA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Hugo\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Quality & Training Manager and Senior IVDR consultant with expertise in CE marking, Clinical Laboratories, SaMD, Precision Medicine, Quality Assurance, and academic lecturing. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Hugo Leis, PhD<\/h3>\n

Training & Quality Manager<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Diego\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Regulatory affairs specialist & CRA with expertise in EU MDR\/IVDR, CE marking, Biological Evaluations (dental), and clinical investigations & technical documentation for MDs & IVDs. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Diego Rodr\u00edguez Mu\u00f1oz, PhD<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \n \n
\n Clinical <\/div>\n
\n EU <\/div>\n\n \n
\n
\n Neuroscience & biotech professional focused on MDR and clinical research strategies for medtech. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Zuzanna Kietlinska<\/h3>\n

Clinical Research Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Callum\n \n \n
\n Clinical <\/div>\n
\n UK <\/div>\n\n \n
\n
\n Experienced clinical affairs professional specialising in performance study submissions and management under IVDR, with a focus on CDx and Precision Medicine. <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Callum Pickett<\/h3>\n

Clinical Alliance Lead<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Grace\n \n \n
\n Regulatory <\/div>\n
\n APAC <\/div>\n\n \n
\n
\n Regulatory Affairs Specialist in MDR & IVDR with expertise in CERs, SVRs, literature review, and regulatory compliance. <\/div>\n <\/div>\n <\/div>\n\n \n
\n
\n

Grace Chia, PhD<\/h3>\n

RA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n

\n
\n \n
\n
\n \"Joana\n \n \n
\n Regulatory <\/div>\n
\n EU <\/div>\n\n \n
\n
\n QA\/RA Specialist supporting teams in clinical evaluations and regulatory compliance with ISO 13485, MDR, and international medical device requirements (FDA, Health Canada, ANVISA). <\/div>\n <\/div>\n <\/div>\n\n \n
\n \n \"LinkedIn\"\n <\/a>\n
\n

Joana Martins<\/h3>\n

QARA Specialist<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n<\/section>\n\n\n

\n
\n \"\"\n <\/div>\n
\n
\n
\n

Vous souhaitez collaborer avec notre \u00e9quipe d'experts ?<\/h2>\n \n <\/div>\n\n
\n \n Rencontrez nos experts <\/a>\n \n Contactez MDx <\/a>\n <\/div>\n <\/div>\n <\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":2,"featured_media":0,"parent":11101,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-12035","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nD\u00e9couvrez l'\u00e9quipe MDx | Experts mondiaux en DIV et technologies m\u00e9dicales<\/title>\n<meta name=\"description\" content=\"D\u00e9couvrez les experts de MDx CRO \u2014 une \u00e9quipe diversifi\u00e9e de sp\u00e9cialistes en DIV et dispositifs m\u00e9dicaux dans les domaines r\u00e9glementaire, clinique et qualit\u00e9 sur les march\u00e9s europ\u00e9ens, britanniques et mondiaux.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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