• Kimberly Hunsicker to lead global growth at D-TARGET

    Good news about the expanded depth, scale, and scope of services offered by our D-TARGET medical devices and diagnostics unit.

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  • Medical device clinical research. That's what we do.

    When it comes to bringing your product to market, you need an experienced and dedicated team that understands the unique nature behind the development and registration of medical devices. Fact is, it's the only thing we do.

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  • Strategic and Regulatory Advisory Services

    D-TARGET offers you the scientific background and regulatory expertise to meet the demands of US and European requirements to successfully set-up and conduct your clinical studies.

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  • Post-Marketing Surveillance
    and Registry Services

    Getting your product to market is good - keeping it there is even better. Let D-TARGET maximize your next PMS or registry trial with cost-efficient solutions adapted to your local capabilities and ressources.

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The CRO dedicated exclusively to medical devices and diagnostics.

We get you quicker to market.

D-TARGET provides you with the therapeutic and functional expertise necessary to help bring your product to market faster than you ever thought possible.

We talk the local language.

Our highly experienced, multi-lingual medical device professionals are located throughout 30 countries around the globe - delivering smooth results in any situation.

We tailor to your needs.

We offer flexible solutions that meet your needs and maximize your study goals throughout the product life cycle. Get what you need - when you need it.

Our services:

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Regulatory Affairs

CE-mark, 510k, PMA, IDE, device classification, de novo and combination drug-device products, submissions

Clinical Trials

Clinical trial set-up, monitoring, CEC/DSMB, biometrics, medical writing, health technology assessment

Post-Marketing Surveillance

Flexible and cost-efficient solutions for your Post-Marketing Surveillance & Registry needs

Global Safety Services

Safety management and medical monitoring plans, safety reporting, SAE, adverse event management

Therapeutic Expertise:

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Cardiology

EP & CRM, Insuffisance Cardiaque, Valves Cardiaques, Intervention Vasculaire, Maladie Cardiaque Structurelle, Greffes Vasculaires

Orthopedics

Degenerative Disc Disease, Cartilage Defect, Partial Hip Replacement/Femur Fracture, Spinal Stabilization, Vertebral Compression Fractures

Gastroenterology

Morbus Chrohn, Gastro-Esophageal Reflux Disease, Gastric Bypass Surgery, Colorectal Surgery, Hernia Repair, Cirrhosis of the Liver

Neuroscience

Cerebral Aneurism, Cerebral Arteriovenous Malformation, Migraine with Aura, Neurovascular Clot, Stroke (Transient Ischemic Attack)

Dedicated exclusively to medical devices and diagnostics.

D-TARGET offers you complete and dedicated support throughout the product life cycle, including:

Exceptional service and customer satisfaction.

Throughout the world, our highly trained, multi-lingual professionals have successfully performed over 250 medical device clinical research projects involving more than 35,000 patients and completed over 90 consultancy projects involving every class of device and therapeutic area.

To learn more about D-TARGET medical device expertise, see here.

In Vitro Diagnostics

D-TARGET provides clinical trial services to help you establish the clinical utility and validity of your products as required for regulatory submission.

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Take the D-TARGET video tour

Discover how D-TARGET can help you maximize your study goals and put you on the pathway to success with this short video presentation.

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Certified ISO 9001 & 13485

D-TARGET is quality certified to meet all US & EU requirements and regulations applicable to the conduct of medical device clinical investigations.

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