Let‘s keep the story short:

We are Qualitätsplan, founded in 2010 and established in Luebeck, Germany.

We offer engineering services for medical device manufacturers in terms of

  • Technical documentation for CE mark
  • Product testing for safety and performance in own test lab
  • Regulatory Affairs support for international markets (US, CAN, AUS,…)
  • Supporting companies from 3-3000 employees

What our customers say

 

«Qualitätsplan compiled the technical documentation - from our perspective – in just the right level of detail.»

Dr. Oliver E. (Product Manager)

 

«Our cooperation with Qualitätsplan was very pleasent. The documentation was compiled accurate and independently.»

Robert T. (Project Manager)

 

«Qualitätsplan ensured - on low level of supervision – the CE conformity of our newly developed product.»

Patrick W. (General Manager)