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We
can take over the following activities for you:
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- MedDRA-coding of data from completed clinical trials
- MedDRA-coding as part of the data management of ongoing clinical
trials
- MedDRA-coding for study reports
- Converting (re-coding) from old data into MedDRA
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The use of MedDRA for reporting
drug safety is a prerequisite for the electronic data transfer with regulatory
authorities.
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Medical Consulting, A-1070 Vienna, Kaiserstrasse 84/10
All rights reserved. Suggestions und tecnical support under |