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Category: Business and Industry
Date Submitted: 09/08/2016 11:57 PM
Biosimilar Market Size, Share, Analysis and Forecast 2016 by
Radiant Insights
Synopsis
Responding to strong desire of overseas and multinational pharmaceutical manufacturers and domestic
pharmaceutical manufacturers to carry out research and development of biosimilar products, this is first time in
history, Chinese pharmaceutical authorities, China Food and Drug Administration officially issued a technical
guidance for development and evaluation of biosimilars and defined the pathway of license approval for
biosimilars. Chinese pharmaceutical authorities require that when conducting the research and development of
biosimilar products in China, the applicant of biosimilar registration application and its sponsor should be in
compliance with the Guidance and follow the pathway of license approval of biosimilars.
How to grasp the opportunity to smoothly conduct the research and development of biosimilar products in China
and speed up your biosimilar product approval time? The overseas and multinational pharmaceutical
manufacturers and their senior executive officers engaging in regulatory affairs must have a comprehensive and
thorough knowledge of the latest Chinese guidance for development, evaluation, license approval of biosimilars,
Browse Complete Summary, Click Here @ http://www.radiantinsights.com/research/latest-chinese-guidancefor-development-evaluation-license-approval-of-biosimilars
Latest Chinese Guidance for Development, Evaluation, License Approval of Biosimilars provided a comprehensive
and thorough knowledge of the latest Chinese guidance for development, evaluation, license approval of
biosimilars and guide you use the Chinese trial venues to keep biosimilars development lean and to smoothly
operate in China.
Summary
China has an indispensable biosimilar market for overseas and multinational pharmaceutical companies. Historical
data shows 40 per cent of China's $1.5bn recombinant biologic product sales come from biosimilars, which...