IDMP Compliance — Get Ready
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IDMP regulations (Identification of Medicinal Products) are currently being finalised by both the European Medicines Agency (EMA) and the Food and Drug Administration (FDA). These regulations will be based on standards created by the International Organisation for Standardisation (ISO). In Europe, these regulations will go into effect in July, 2016. Read on to find out more about the position of the FDA, what is included in the standards, and what the implementation of IDMP will require from all divisions and branches of pharmaceutical companies.
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