Coding of the study data

A prerequisite for the electronic data exchange with regulatory authorities is the use of a coding system. “Medical Dictionary for Regulatory Activities” (MedDRA) represents the recognised coding standard, especially in the pharmaceutical industry. 

Apart from that, we also offer coding according to ATC, WHO, etc. 

We will take over the following activities for you:
  • Coding of data from completed clinical trials according to MedDRA, ATC, WHO, etc.
  • Coding of data as part of data management of currently ongoing clinical trials
  • Converting (re-coding) of data from a previous state into MedDRA
  • MedDRA coding of data for preparation of the study report