We partner with medical device and IVD firms to support quality assurance and regulatory affairs needs. We offer more than 30 years experience working with regulatory affairs agencies globally on a variety of risk class products. Let us help you develop and execute a regulatory affairs and compliance strategy to meet your company goals.
Company’s Keywords:
eu mdr, fda class i, apac, ii & iii medical devices, eu & north america expertise, latam
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medical devices
2004
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