Latest Regulations on Pharmaceutical International Multi-Center Clinical Trials in ChinaAccess China Management Consulting Ltd. - March 19, 2015 - 101 Pages - SKU: ACCH5499504 |
Countries covered: China
Latest Regulations on Pharmaceutical International Multi-Center Clinical Trials in China
This is first time in history, Chinese pharmaceutical authorities officially issued a guidance on international multi-center clinical trials of drugs in China, which has begun to be implemented on March 1, 2015. The guidance provides an opportunity to reduce risk from the examination uncertainty and approval delays to eat up your time and energy to achieve a successful entry into such a lucrative drug market, and to avoid trouble for your business smoothly in China. The overseas and multinational pharmaceutical manufacturers must be compliance with the latest regulations.
... read the full abstract
Latest Regulations on Pharmaceutical International Multi-Center Clinical Trials in China
This is first time in history, Chinese pharmaceutical authorities officially issued a guidance on international multi-center clinical trials of drugs in China, which has begun to be implemented on March 1, 2015. The guidance provides an opportunity to reduce risk from the examination uncertainty and approval delays to eat up your time and energy to achieve a successful entry into such a lucrative drug market, and to avoid trouble for your business smoothly in China. The overseas and multinational pharmaceutical manufacturers must be compliance with the latest regulations.
... read the full abstract
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