Mar.16,2010

Venlafaxine (150mg) ER Capsule full BE study for registration with SFDA was completed.

Dec.15,2009

Sulfadoxine/Pyrimethamine(250mg/25mg) co-blistered tablet's efficacy/safety part of the dossier (BE study) submitted to the WHO Pre-Qualification of Medicines Programme is considered acceptable by WHO.

Jun.30,2009

Felodipine(5mg) ER capsule full BE study for registration with SFDA was completed.


 

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Vivo Development Ltd. is a Clinical Research Organization specialized in phase I clinical development studies, including bioequivalence, pharmacokinetics, first-time in human studies (FIH), formulation comparisons, food-drug and drug-drug interactions, and metabolism studies. We are based in Shanghai and conduct our clinical studies in Chinese SFDA approved phase I units in Shanghai and other cities.

We aim to provide early clinical development services to clients with a full spectrum of registration needs, including ANDA with the US FDA, MA with the EMEA, PQ with the WHO, and new product registration with the Chinese SFDA.

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