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Simulations Plus Inc. received an order from China’s drug evaluation agency to license its GastroPlus product. Financial terms of the deal between the Lancaster drug modeling software developer and the Center for Drug Evaluation of the National Medical Products Administration in China were not disclosed. John DiBella, Simulations Plus division president said, the company has cultivated relationships with different institutions affiliated with China’s National Medical Products Administration to use its technology for the evaluation of drug specifications and bioequivalence. “Now, researchers at the CDE will add GastroPlus to serve as a key platform for model-informed drug development to aid regulatory reviews,” DiBella said in a statement. “This news is welcomed by over 20 (and growing) domestic Chinese pharmaceutical companies and research hospitals that have been employing our technologies.”

Mark madlerJohn dibellaChina national medical products administrationChinese drug agency licenses simulations plus softwareSimulations plus incChinese drug agency licenses simulations plusDrug evaluationNational medical products administrationSimulations plusஜான் டிபெல்லாஉருவகப்படுத்துதல்கள் ப்லஸ் இன்க்மருந்து மதிப்பீடுஉருவகப்படுத்துதல்கள் ப்லஸ்