ABOUT US
QMedCo is a boutique consultancy firm that specialises in providing strategic advice on Clinical Evaluation to the medical device industry to achieve efficient clinical trials that produce robust clinical data to fully comply with the European MDR to achieve CE mark. QMedCo has extensive experience in clinical evaluation & performing clinical trials.
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SERVICES
QMedCo provides consultancy services to medical device companies to strategically advise on their Clinical Development Plans to achieve efficient clinical trials that comply with the European MDR regulations.
We strategically consult on the pre clinical phase, on the clinical stage and post marketing clinical follow up.
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NEWS
Our News section keeps you informed of the latest news, events, and regulations in the medical technology world.
From conferences and conventions to updates and regulatory developments, our News section will help you stay ahead of the curve. We monitor the industry, and will provide you with the latest and most relevant information.
PARTNER
Our CE Consultancy works with a strategic partner to ensure that we cover the whole regulatory process.
Together we provide valuable insight and knowledge to help our clients reach compliance quickly and efficiently.
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