We’re passionate about medical devices and IVDs.

With over 30 years of experience in managing medical device clinical investigations and IVD performance around the globe, we have what it takes to move your product to market swiftly and cost-effectively, saving you precious time and money in the process.

Our unsurpassed clinical and regulatory expertise in medical device and IVD market access means you avoid the unnecessary delays and unexpected problems that affect eight out of ten product registrations in the world today.

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Your partner for global medical device clinical investigations or IVD performance studies and market access.

Clinical Investigations

Global clinical expertise with local, quality monitoring and project management.

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PMCF

Optimization of your costs for post-market clinical follow up activities.

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Regulatory Affairs

Providing regulatory and clinical strategies for global market access.

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Our Achievements

400+ clinical investigations successfully set up and completed world wide

Over 200 CEP/CER written and submitted

Over 30 successfully passed MDR without major comments

Proven track record in class III medical device registrations without hurdles

Success to CE-mark is absolutely predictable to us from start to finish!

Global use of clinical data

Successful foreign data justifications

Saving millions for our clients

Discover how we can get your medical device to market faster

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We're hiring!Clinical Research Associates needed in Belgium, Netherlands, France, Switzerland, and UK.

Are you a nurse, or a paramedical professional, looking to change your career for something exciting and rewarding? If so, MD-Clinicals has the opportunity you’ve been waiting for in the fascinating world of medical device clinical research.

Become a Clinical Research Associate at MD-Clinicals