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25 Sep 2009 ... E-mail: mail EMEA. Europa.EU http://www.emea.europa.eu .... health care professionals to report the following adverse .... ://www.emea.europa.eu/pdfs/ human/few/50344907en.pdf).
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general-emea3593812009 - ema europa is a regulatory filing required by the European Medicines Agency (EMA) for certain pharmaceutical products.
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Manufacturers and distributors of pharmaceutical products in the EMEA region are required to file general-emea3593812009 - ema europa.
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The purpose of general-emea3593812009 - ema europa is to ensure the safety, quality, and efficacy of pharmaceutical products in the EMEA region.
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Information such as product data, manufacturing process, safety data, clinical trial results, and adverse event reports must be reported on general-emea3593812009 - ema europa.
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