UKCA and CE Marking, MHRA Medical Device Regulatory Consultant
États-Unis
Anglais, Espagnol, Allemand
Certaines informations sont présentées en anglais.
À propos de moi
Welcome to my profile. I provide professional regulatory compliance support for manufacturers, startups, importers, and businesses seeking UK and EU market access. I specialize in UKCA compliance, CE marking, MHRA medical device registration, EU MDR documentation, Declaration of Conformity, technical file preparation, and ISO 13485 documentation support. My services include product classification, regulatory document review, compliance gap assessments, and practical guidance tailored to your product and target market. I prioritize accuracy, confidentiality, clear communication, and reliable.... Plus d’infos