Our clinical research team specializes in crafting and implementing robust evidence plans that align with your diagnostic design and development project, even if the IVD products were created independently of Eclevar.
Our IVD Clinical Research Services offer a comprehensive approach to clinical and regulatory strategy, specimen procurement, regulatory application assistance, IRB management, supply administration, biostatistics solutions, site oversight, and a combined research and design department. Trust us for success in IVD research.
Eclevar clinical research organization specializes in comprehensive management of point-of-use diagnostic device research programs. From initial concept development to regulatory submission, our team is dedicated to delivering the crucial data necessary for a successful market entry. We prioritize adherence to both local and international standards, including Good Clinical Practice (GCP) guidelines and Good Laboratory Practice (GLP) principles.Â
Our team meticulously analyses your product to develop regulatory pathways that are tailored to your specific needs. With our expertise, we create a formal roadmap that you can rely on, allowing you to validate your point-of-use device at an early stage in the research and development process.Â
We have established a strong network of reliable service providers who specialize in procuring high-quality specimens. By working with us you can focus on the core aspects of your research and development while we ensure a seamless and efficient process of specimen acquisition.Â
Our Eclevar experts will answer your questions and guide you through the next steps!
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ECLEVAR FRANCE:
231 rue Saint-Honoré, 75001 Paris, France
ECLEVAR GMBH
ERFURT, Erfurt Hauptbahnhof
4th, 5th floor
Bahnhofstr. 38 Erfurt 99084
ECLEVAR Australia
Umina Beach NSW 2257, Australia
ECLEVAR UK Limited
3rd Floor 207 Regent Street, London, W1B 3HH
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