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Titlebook: China Food and Drug Law; Policy, Practice, an John C. Balzano Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusive li

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發(fā)表于 2025-3-21 17:56:59 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱China Food and Drug Law
副標(biāo)題Policy, Practice, an
編輯John C. Balzano
視頻videohttp://file.papertrans.cn/243/242092/242092.mp4
概述Provides full coverage of Chinese Food and Drug Regulation.Combines theory, policy, and practice into one discussion.Usable by experts but also user-friendly for those with no experience
叢書(shū)名稱Law for Professionals
圖書(shū)封面Titlebook: China Food and Drug Law; Policy, Practice, an John C. Balzano Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusive li
描述.This book is an analysis of policy and law governing the development, approval, manufacture, distribution, marketing and post-market surveillance of human drugs, medical devices, foods and cosmetics in Mainland China (“China FDD Regulation”)...It analyzes the policy and general principles behind China FDD Regulation, including the history and jurisdiction of the central and local agencies that administer the laws and regulations, the administrative law structure in which these agencies operate, and other aspects of FDD Regulation interpretation and enforcement. ?Although it describes practice in China, this book is written in the comparative perspective (i.e., sensitive to assumptions made by those who are steeped in FDD Regulation in the U.S., Japan, and the EU)...It includes one chapter on each regulatory space (drugs, medical devices, cosmetics, and food) organized by the lifecycle of products. It also covers subcategories of products, such as vaccines, radiopharmaceuticals, and in vitro diagnostic medical devices. The book includes specialty chapters on areas that are common to multiple types of regulated products, such as biosecurity and advertising...It is the first English
出版日期Book 2024
關(guān)鍵詞Chinese Food Law; Chinese Drug Law; Human drugs; Cosmetics; Medical devices; China FDD Regulation; Biosecu
版次1
doihttps://doi.org/10.1007/978-3-031-61901-4
isbn_softcover978-3-031-61903-8
isbn_ebook978-3-031-61901-4Series ISSN 2662-141X Series E-ISSN 2662-1428
issn_series 2662-141X
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

書(shū)目名稱China Food and Drug Law影響因子(影響力)




書(shū)目名稱China Food and Drug Law影響因子(影響力)學(xué)科排名




書(shū)目名稱China Food and Drug Law網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱China Food and Drug Law網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱China Food and Drug Law被引頻次




書(shū)目名稱China Food and Drug Law被引頻次學(xué)科排名




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發(fā)表于 2025-3-21 20:15:34 | 只看該作者
Designing Effective Content Marketing Postsin China. These laws not only control promotional content, but also influence informational and scientific exchanges, as well as the design and review of labels and package inserts in all the product spaces discussed in the preceding chapters. This Chapter is a discussion of this area and its unique features.
板凳
發(fā)表于 2025-3-22 01:57:23 | 只看該作者
John C. BalzanoProvides full coverage of Chinese Food and Drug Regulation.Combines theory, policy, and practice into one discussion.Usable by experts but also user-friendly for those with no experience
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發(fā)表于 2025-3-22 05:26:45 | 只看該作者
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發(fā)表于 2025-3-22 20:32:02 | 只看該作者
Adverse Events with Biomedicinessdiction, and key parts of their roles in creating food, drug, device, and cosmetic regulatory policy and regulations and in implementing and enforcing those regulations. This chapter devotes particular time to the history, internal structure, and affiliated centers for drug and device evaluation of
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發(fā)表于 2025-3-22 22:10:33 | 只看該作者
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發(fā)表于 2025-3-23 04:58:10 | 只看該作者
https://doi.org/10.1007/978-88-470-5313-7ossible to discern common principles and trends that pervade them. This chapter provides an introduction to these common elements to assist with understanding the specific analyses for each area that follow. By looking at the commonalities, it is possible to begin to understand China’s overall FDD r
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發(fā)表于 2025-3-23 07:32:13 | 只看該作者
Adverse Events with Biomedicinesn over the life cycle of a drug, from development to the post-marketing environment. From 2015 to 2023, China has taken steps to transform itself from a generic drug market to an innovative one, where the latest medicines are available. To facilitate this change, it has tried to harmonize its drug r
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