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.
- 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