Provider Country:
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Bulgaria
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Sofia University
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Provider Country:
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Czech Republic
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University of Olomouc (Institute of Molecular and Translational Medicine)
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Provider Country:
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Finland
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University of Helsinki (Institute for Molecular Medicine)
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Provider Country:
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France
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CEA-NeurATRIS
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Provider Country:
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Italy
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Istitute Superiore di Sanita
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Provider Country:
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Latvia
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Riga Stradins University
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Provider Country:
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Luxembourg
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Integrated Biobank of Luxembourg
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Provider Country:
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Netherlands
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Amsterdam University Medical Centre
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Provider Country:
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Norway
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University of Oslo (Centre for Molecular Medicine)
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Provider Country:
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Portugal
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INFARMED
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Provider Country:
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Slovenia
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University of Ljubljana
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Provider Country:
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Spain
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Vall d'Hebron Research Institute
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Provider Country:
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Sweden
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Uppsala University
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Addressing regulatory issues is an integral part of bio medicinal development, and their importance will only continue to increase for the foreseeable future. The EATRIS regulatory service and support centre is available to help guide you through this complex world, especially for complex and hybrid products for which clear regulatory guidance may not be available. Early assessment of the potential requirements may prevent unnecessary project delays, reduce extra costs and most importantly prevent penalties resulting from non-adherence to legal requirements. Through a combination of in-house and external partnerships with a range of regulatory experts and groups, EATRIS can provide regulatory support for most types of product. Our range of services include: - Expert opinion - Orphan Drug Designation and Scientific Advice application at the EMA - Pre-clinical and clinical plan development - Informal scientific advice with selected national competent authorities, for highly complex projects This service is a fee-based service available for academia and industry. Please contact info@eatris.eu for more information.
Biomedical laboratory equipment for the product categories ATMPs, Biomarkers, Imaging and Tracing, Vaccines and Small Molecules.