Your Trusted Expert in EU Medical Device Regulation

At Health Tech Guardian, I specialize in guiding medical device companies through the complexities of the European Union’s Medical Device Regulation (MDR). With a focus on patient safety, regulatory compliance, and the empowerment of clinical research professionals, I help bring innovative medical devices to market in a responsible and effective way.

MDR SERVICES

See how my services simplify EU Medical Device Regulation for you.

MDR NEWS

Stay informed with expert insights, regulatory updates, and practical tips on navigating EU MDR.

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✉️ Find all my contact details here

Core values of Health Tech Guardian

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Ensuring Safe Clinical Trials

I collaborate closely with sponsors and stakeholders to ensure that clinical trials for medical devices are conducted in strict compliance with EU MDR, prioritizing safety and ethical standards at every step.    
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Patient-Centered Focus

At Health Tech Guardian, the voice of the patient comes first. I commit to ensuring that patient safety, health, and well-being are central to every clinical trial and regulatory decision.
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Supporting Professional Growth

I am dedicated to the personal and professional development of Clinical Research Coordinators (CRC). My goal is to empower them with the knowledge and skills necessary to navigate the regulatory landscape and succeed in their roles.

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