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CE Certification Consultants for Medical & IVDs Devices
We provide CE certification consultancy services to obtain CE marking for your products under the EU MDR 2017/745 and EU IVDR 2017/746 regulations.
CE Certification for Contact Lenses
Detailed guide that explores the standards and processes of CE certification for contact lenses. Learn about the requirements and what they mean for you.
UKCA Mark Technical File Consultancy
Maven Profserv helps you in establishing products in various countries with experienced regulatory consulting. Visit mavenprofserv.com for details.
MHRA Registration for Medical Device UKCA Certification
MHRA Registration database details include manufacturer name, address, MHRA reference number, and registered devices. Renewal is required one year after initial registration or confirmation, and every two years thereafter. Failure to renew may…