Equipment qualification is an activity which has been mandadory since the late 80s. In the meantime IT documentation systems are widespread. Nevertheless, most of the documentation in pharmaceutical companies is still paper based, especially regarding qualification. Even if companies get the qualification documentation from their suppliers electronically, very often it is printed out. Is this necessary? Wouldn´t a completely electronic documentation sytem work for both parties (supplier and customer)? This we want to know. The following survey just has 13 questions and will thus only take you about 10 minutes. No personal data will be collected - your answers are of course anonymous. And you will find the results of the survey in one of the coming newsletters.