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In some cases, you may need to conduct a clinical investigation in China to meet the CFDA's clinical data requirements. Identifying your route to conformity up front will save you time, resources, and frustration during the NMPA registration process. There are two clinical conformity routes: Clinical Evaluation Report (CER)

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The China Food and Drug Administration (CFDA) released a detailed report on inspections conducted throughout the last year. A total of 431 inspections including pre-approval inspections, GMP certification inspections, GMP follow-up inspections, unannounced inspections, overseas inspections, GSP unannounced inspection and inspection observations are analysed therein.
 

 

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The .gov means it’s official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site. Federal Expenditures by CFDA Number Enterprise Report Purpose: The purpose of this report is to provide assistance to agencies when preparing the Federal Financial Assistance Direct Disclosure Form. The intended users for this report are agencies that currently use or would like to use the CFDA field in AFRS.
 
 

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China’s State Food and Drug Administration (CFDA China, 国家药品监督管理局, renamed to National Medical Products Administration or NMPA China in 2018) is Chinese government’s administrative body responsible for regulating pharmaceuticals, medical devices, and cosmetics in China. 1 day ago · The report pointed out that people will consume more than 102 million tons of clothing over the next decade — up 60 percent from 2020 — and 80 percent of it will end up in landfills.

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Contact Information. Lori Washington 1400 Independence Avenue, SW Room 4204 Mailstop 3226, Washington, District of Columbia 20250 Email: [email protected] Phone: 202-720-1400

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