IPRF, LLC

We provide FDA-EU RA/QA Compliance/Training assistance & Intl Med Device/IVD/Pharma product registration assistance. We can cut registration time by 2 months

  • Stage Full Product Ready
  • Industry Consulting
  • Location San Diego, CA, US
  • Currency USD
  • Founded May 2013
  • Employees 2
  • Website intlproductreg.com

Company Summary

IPRF, LLC is a consulting firm whose focus is to provide assistance to pharmas, medical device and IVD companies to obtain and/or maintain RA/QA compliance to FDA/OUS regulations & legalization of documents for foreign use.
Services:
FDA/ISO RA/QA Consulting
GxP Compliance/Registration Assist/Training/Audits
Quality System Development
Legalization Svcs:
Notary Svcs
State/Embassy Legalizations

Team

  • Marie Dorat, CQA, CAA, Notary Public
    CEO

    12 years experience working with Medical Device/IVD/Pharmas:
    Develop, Implemented and maintained Quality Management Systems
    Intl product registration specialist – Notary & Certified Apostille Agent-50 states
    Lead GCP, GLP, cGMP, ISO(13485, 14001, 14971, 17025, 9001), OSHA, ITAR & AS9100 audits in the US/EU
    Developed/implemented company-wide compliance training programs & online webinars

Starting a startup?

Join the world's largest startup network for guidance, tools, and fundraising opportunities.

Get Started for Free