Conformity Assessment
A CE mark shows that a medical device meets the General Safety and Performance Requirements of the EU regulations for in vitro diagnostics (EU) 2017/746 and medical devices (EU) 2017/745.
As Notified Body 2962, QMD Services issues CE certificates following successful conformity assessment. We accept technical documentation in English and German, and our scope is published in the NANDO database.
Before You Enquire
Four Quick Steps
Check our scope in NANDO
Confirm that your device falls within QMD Services' designation.
Understand the process
Read through each stage on our Your Way to Certification page.
Review costs and services
See how CE marking fees are structured on our Costs & Services page.
Apply online
Send us your enquiry, email us at info@qacamail.com or call us at +91 95996 19392.
How We Work With You
A Structured Dialogue From Day One
Innovative Devices Get Certified With QMD
Start the conversation today and our team will guide you through the next steps.
