Certara®, the global leader in model-informed drug development, regulatory science, real-world evidence and market access services, today announced that Brazil’s National Health Surveillance Agency (ANVISA), Japan’s Pharmaceuticals and Medical Device Agency (PMDA), and the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) are increasing their adoption of Certara’s Phoenix® software to evaluate drug regulatory submissions.
April 4, 2019
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