"A new version of the Medical Dictionary for Regulatory Activities (MedDRA) has just been released. This blog post will provide a brief introduction to MedDRA and next week I’ll look at some of the changes in version 19.0, published in English on 2 March and in other languages today.
What is MedDRA?
MedDRA is the acronym for Medical Dictionary for Regulatory Activities. It’s an international medical terminology used by the pharmaceutical industry, medical device industry and regulatory agencies throughout the drug development process, in clinical trials and for postmarketing activities such as pharmacovigilance (periodic safety update reports and adverse drug reactions), clinical reports, data presentation and ..."
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