On Feb. 2, 2019, the European Medicines Agency announced that companies that make angiotensin II receptor blockers must review their manufacturing practices to prevent the production of products containing nitrosamine impurities, N-nitrosodimethylamine (NDMA) and N nitrosodiethylamine (NDEA)Original Article
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David Miller
a pharmacist, a tech enthusiastic, who explored the Internet to gather all latest information pharma, biotech, healthcare and other related industries.