Generics medicines in the European Union

| March 18, 2018

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The European Medicines Agency (EMA) assesses applications from companies to market generic medicines in the European Union (EU). A generic medicine is developed to be the same as a medicine that has already been authorised, called the reference medicine. A generic medicine contains the same active.

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Derex Labs Pvt.Ltd

To cater the "trained human resources" needs of Global Pharmaceutical Industry by providing value based training in concepts of pharmaceutical industry (like cGMP, GLP, GAP, GCP, Regulatory Affairs, Instrumental Analysis( HPLC,GC,UV,IR),Method Development, Method Validation, Research & development etc) and soft skills.

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