MeddiQuest Regulatory Affairs Limited

medical devices

About

MeddiQuest Regulatory Affairs is your organization for all your Regulatory and Quality needs to bring innovative Hi-tech medical products to the EU. UK and US Markets. MeddiQuest have over 20 years experience and have been doing business in Ireland for over 6 years in assisting our customers to prepare validation activities and submission files for new and updated software as stand-alone, an accessory to a device or embedded into the device. MeddiQuest also provide special expertise in bringing medical devices with an ancillary medical function to the European Market and developing consultation documentation. Together with our partners in Pharmaceutical Regulation we similarly advise a devices ancillary to a medicine.

Technologies

Apache WordPress.org Remote

Keywords

samd hitech devices eu authorised representative software as a medical device quality management innovation combination products notified body selection startup business regulatory affairs european regulation euar uk regulation risk management audit management usa regulation system design product registration medical device regulation healthcare regulatory consultancy for medical devices medical device registration ireland other scientific and technical consulting services regulatory approval quality management systems regulatory consulting regulatory submission support regulatory strategy medical devices ce marking

Location

40-44 Patrick Street, Waterford, Waterford, Ireland, X91 X3KF

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