Our training content is developed with the aim to summarize and comprehensively present you with demanding contents in the field of clinical studies on medicinal products and medical devices as well as medical devices regulation.

Our trainings, delivered as workshops or web-based trainings, are set in a way which enables to provide a proper and an efficient training to participantsof our trainings. Each training ends with a knowledge test. Test consists of 20 random selected questions. One must achieve 80% of correct responses to earn the training certificate.

Trainings allow you to obtain a training certificate at a reasonable price and are intended for investigators and their clinical research teams, representatives of clinical trials sponsors and manufacturers of medical devices.

Currently we offer the following trainings:

1. 1. ICH E6(R2) GCP Investigator Site personnel training (Good Clinical Practice in Slovenian language; in compliance with the requests of TransCelerate BioPharma)

1. 2. ICH E6(R2) GCP Investigator Site personnel training (Good Clinical Practice in English language; in compliance with the requests of TransCelerate BioPharma)

1. 3. ICH E6(R2) GCP training (in English language; CRA, Projects Managers, Clinical Institutions performing academic studies and Investigator Initiated clinical studies)

1. 4. EU Medical Devices Regulation 2017/745 (in Slovenian language)

To upgrade your knowledge choose an eLearning course on the right or contact as at info@adax.si or +386 (0)59 710 255 for a training in the form of a workshop.