Through our strategic alliance partners, we help our clients with product registration and clinical trials of pharmaceuticals and medical devices in China. We manage the whole registration process, including:
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Translation and preparation of registration dossier |
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Technical and non-technical communication to medical opinion leaders |
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Monitoring and management of clinical trials |
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Lobbying on evaluation committee members and government agencies |
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Other administrative duties and pubic relations work |
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While we can not guarantee final registration approval, our expertise in this field does help and our past registration success rate has been 100%. |
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