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Concept paper on good genomics biomarker practices

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Originally posted on DRUG REGULATORY AFFAIRS INTERNATIONAL:

Document details

http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2014/08/WC500170682.pdf

Download document Concept paper on good genomics biomarker practices
Reference number EMA/CHMP/PGWP/415990/2014
Status draft: consultation open
First published 04/08/2014
Last updated 04/08/2014
Consultation start date 04/08/2014
Consultation end date 04/11/2014
Email address for submissions pgwpsecretariat@ema.europa.eu

Summary

Genomic data have become important to evaluate efficacy and safety of a drug for regulatory approval. As a result, genomic information has been increasingly included in drug labels relevant for the benefit/risk evaluation of a drug and consequently as guidance for patient treatment.

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