MedTech

We have a particular interest in global labelling, regulatory affairs, and human factor testing of home-use devices and device-software applications. Services in this area include:

• Instructions for Use (IFU) writing, developing and pre-testing on potential users.

  
  

• Development and pre-testing of supporting educational materials for medical devices.

  
  

• Consumer evaluation of medical device labelling documentation.

  
  

• Global label regulatory reviews.

  
  

• Device software and apps testing.

  
  

• Human factor testing of home-use medical devices.

  
  

• Content creation and usability testing of digiceuticals.