Home > Newsletters > Drug Industry Daily > EMA Offers Guidance on Marketing Applications for Transdermal Patches
Drug Industry Daily
Sept. 17, 2012 | Vol. 11 No. 182
EMA Offers Guidance on Marketing Applications for Transdermal Patches
Manufacturers of transdermal patches should minimize the amount of residual drug substance in the patch as much as possible to avoid patient and environmental safety risks, according to a new European Medicines Agency (EMA) draft guideline.
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnewsAll rights reserved. Do not duplicate or redistribute in any form.