About
QUAlity & REGulatory expertise EU Region Medical devices regulatory and quality activities - Regulatory Expertise - Regulatory Intelligence - Technical documentation writing and review - Assistance with CE conformity activities - Assistance with Quality Management System activities according to EN ISO 13485 - Internal audits and suppliers audits - Trainings on MDR 2017/745 - EN ISO 13485 - PRRC - combined MDs-Medicinal Products - Economic Operators roles Middle-East Region Quareg Consulting can also provide support in medical devices in Middle East: o Medical Devices regulatory activities (registrations, variations, etc.) o Vigilance system implementation o Quality Management System (Quality Manual, Quality policy, procedures, audits, etc.)
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Company Information
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Employees 1
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Founded 2020
Location
Massy, Ile-de-France, France
