D-TARGET provides you with the therapeutic and functional expertise necessary to help bring your product to market faster than you ever thought possible.
Our highly experienced, multi-lingual medical device professionals are located throughout 30 countries around the globe - delivering smooth results in any situation.
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.
CE-mark, 510k, PMA, IDE, device classification, de novo and combination drug-device products, submissions
Clinical trial set-up, monitoring, CEC/DSMB, biometrics, medical writing, health technology assessment
Flexible and cost-efficient solutions for your Post-Marketing Surveillance & Registry needs
Safety management and medical monitoring plans, safety reporting, SAE, adverse event management
EP & CRM, Insuffisance Cardiaque, Valves Cardiaques, Intervention Vasculaire, Maladie Cardiaque Structurelle, Greffes Vasculaires
Degenerative Disc Disease, Cartilage Defect, Partial Hip Replacement/Femur Fracture, Spinal Stabilization, Vertebral Compression Fractures
Morbus Chrohn, Gastro-Esophageal Reflux Disease, Gastric Bypass Surgery, Colorectal Surgery, Hernia Repair, Cirrhosis of the Liver
Cerebral Aneurism, Cerebral Arteriovenous Malformation, Migraine with Aura, Neurovascular Clot, Stroke (Transient Ischemic Attack)
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.
D-TARGET provides clinical trial services to help you establish the clinical utility and validity of your products as required for regulatory submission.
Discover how D-TARGET can help you maximize your study goals and put you on the pathway to success with this short video presentation.
D-TARGET is quality certified to meet all US & EU requirements and regulations applicable to the conduct of medical device clinical investigations.