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Who are we?
European Medicines Registration Consultancy is an established pharmaceutical consultancy company offering an extensive range of regulatory affairs and compliance services to both Irish and international pharmaceutical, medical device and related industries.
Where are we?
EMRC is based in Ireland thus is strategically located to facilitate companies in the European Union and the United States.
What do we do?
EMRC aims to provide a comprehensive, high quality service, tailored to meet each client’s individual needs. The service includes consultancy and practical assistance to pharmaceutical, medical device, functional food, herbal/homeopathic and cosmetic companies as well as pharmaceutical wholesalers and manufacturers. EMRC specialises in the preparation and management of Product Authorisation application submissions to the Irish and European regulatory authorities (Nationally and through the Mutual Recognition Procedure (MRP) and Decentralised Procedures (DCP)). EMRC also provides guidance to clients on planning, developing and implementing a quality management system to ensure compliance with ISO, Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) standards.