The CFDA issued a public solicitation of opinions on the adjustment of the review and approval of drug clinical trials (draft for comments).
In order to implement the requirements of the General Office of the CPC Central Committee and the General Office of the State Council on Deepening the Reform of the Review and Approval System and Encouraging the Innovation of Drugs and Devices, the CFDA organized and drafted the Announcement on Adjusting the Review and Approval of Drug Clinical Trials (Draft for Comments), which is now open for comments and suggestions.
Relevant units and individuals are requested to give feedback by email before January 14, 2018.
In order to encourage innovation, accelerate the creation of new drugs, and meet the public's drug needs, in accordance with the Opinions of the General Office of the CPC Central Committee and the General Office of the State Council on Deepening the Reform of the Review and Approval System and Encouraging the Innovation of Drugs and Devices (Hall Zi  No. 42), optimize the review and approval of drug clinical trials, learn from international experience, and adjust the procedures and methods of clinical trial review and approval.
In order to ensure the quality of non-clinical evaluation research of drugs and protect public use, the State Food and Drug Administration recently issued the newly revised "Good Management Practice for Non-clinical Research of Drugs" (Order No. 34 of the State Food and Drug Administration) (hereinafter referred to as the "Specification")
The 2019 New Delhi International Pharmaceutical Raw Materials Exhibition (CPHI) will be held on November 26-28 at Greater Noida International Exhibition Center, New Delhi, once a year, is a well-known international pharmaceutical raw materials event in India, and is also a must for enterprises from all over the world in this field to explore the Indian market.
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