AR Questionnaire

Your Name(*)
Please let us know your name.

Your Email(*)
Please let us know your email address.

Company Name(*)
Invalid Input

Country(*)
Invalid Input

Website
Invalid Input

Phone #
Invalid Input

Subject(*)
Please write a subject for your message.

Message(*)
Please let us know your message.

Device Information (if applicable):

Invalid Input

Regulatory Services

Invalid Input

Invalid Input

Project Management

Invalid Input

Invalid Input

Please upload the following documents (If applicable)
Invalid Input

Invalid Input

Invalid Input

Invalid Input

Invalid Input

Invalid Input

Invalid Input

Please enter the characters you see in this picture(*)
Please enter the characters you see in this picture
  RefreshInvalid Input

News

  • (EU) Regulation 2024/1689, the so-called "AI Act" (AIA), and the MDR/IVDR
    Software (including AI) for medical purposes is regulated in Europe and the United Kingdom as a medical device. It requires comprehensive assessment before being placed on the EU and UK market under Medical Device Regulations (MDR) and the EU In Vitro Diagnostic Medical Devices Regulation (IVDR). The European Union (EU) has introduced new legislation on…

Whitepaper