派博傳思國際中心

標題: 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 [打印本頁]

作者: 瘦削    時間: 2025-3-21 17:56
書目名稱China Food and Drug Law影響因子(影響力)




書目名稱China Food and Drug Law影響因子(影響力)學科排名




書目名稱China Food and Drug Law網(wǎng)絡(luò)公開度




書目名稱China Food and Drug Law網(wǎng)絡(luò)公開度學科排名




書目名稱China Food and Drug Law被引頻次




書目名稱China Food and Drug Law被引頻次學科排名




書目名稱China Food and Drug Law年度引用




書目名稱China Food and Drug Law年度引用學科排名




書目名稱China Food and Drug Law讀者反饋




書目名稱China Food and Drug Law讀者反饋學科排名





作者: 同謀    時間: 2025-3-21 20:15
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.
作者: 變化無常    時間: 2025-3-22 01:57
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
作者: nonsensical    時間: 2025-3-22 05:26

作者: 施魔法    時間: 2025-3-22 12:48

作者: Arb853    時間: 2025-3-22 16:06

作者: Arb853    時間: 2025-3-22 20:32
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
作者: 急性    時間: 2025-3-22 22:10

作者: 大看臺    時間: 2025-3-23 04:58
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
作者: insightful    時間: 2025-3-23 07:32
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
作者: 使激動    時間: 2025-3-23 10:00
https://doi.org/10.1007/978-88-470-5313-7el of medical technology approved for use in health care in China. It discusses the general procedures and requirements for pre-market approval and risk-based regulation over the life cycle of devices, into the post-market environment. It also examines more specific methods for regulating certain ty
作者: 廣大    時間: 2025-3-23 15:34

作者: BIAS    時間: 2025-3-23 21:19

作者: Gum-Disease    時間: 2025-3-24 01:37

作者: babble    時間: 2025-3-24 02:22
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
作者: 粘連    時間: 2025-3-24 09:09
https://doi.org/10.1007/978-3-031-61901-4Chinese Food Law; Chinese Drug Law; Human drugs; Cosmetics; Medical devices; China FDD Regulation; Biosecu
作者: 圣人    時間: 2025-3-24 13:43

作者: Negligible    時間: 2025-3-24 18:43

作者: linear    時間: 2025-3-24 20:28
Common General Principles of China Food and Drug Regulation,These general principles also relate to many of the trends described in the Introduction, including decreasing and streamlining onerous pre-market approvals, adopting a regulatory approach that looks at safety, quality, and effectiveness over the product’s lifecycle, enhancing post-market safety controls, and promoting innovation.
作者: FLEET    時間: 2025-3-24 23:38
Book 2024human 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 administrat
作者: avulsion    時間: 2025-3-25 05:36
Agency Jurisdiction Over Food and Drug Law, the National Medical Products Administration, which plays the primary national role in the regulation of drugs (small molecule drugs and biologics), medical devices and cosmetics, and similar attention to the divisions and affiliated food evaluation center of the State Administration for Market Regulation, which regulates finished food products.
作者: bacteria    時間: 2025-3-25 09:13
Biosecurity and FDD Research and Development, most prominent role in this area in China are the human genetic resource (HGR) regulations. This chapter examines the development of the area of biosecurity overall, with particular attention to the HGR regulatory regime.
作者: bizarre    時間: 2025-3-25 14:11

作者: Gesture    時間: 2025-3-25 19:41
Cosmetics Regulation in China,ncreasingly mainstream online sales. But the regime still contains requirements and processes that are onerous, particularly as compared to other jurisdictions. This chapter explores the recent evolution and the current state of affairs.
作者: Morphine    時間: 2025-3-25 21:28

作者: aphasia    時間: 2025-3-26 00:26
Administrative Law Concepts and Enforcement Powers,ve agencies and through the courts. This chapter discusses the ways in which enforcement begins, the collection of different types of evidence and their different persuasive values within the system, and the appeal process.
作者: CRUDE    時間: 2025-3-26 05:26

作者: slow-wave-sleep    時間: 2025-3-26 10:03
Medical Device Regulation,sk-based regulation over the life cycle of devices, into the post-market environment. It also examines more specific methods for regulating certain types of devices, including digital health products, through specific standards and, more recently, technical guidelines.
作者: deficiency    時間: 2025-3-26 13:50
Adverse Events with Biomedicines the National Medical Products Administration, which plays the primary national role in the regulation of drugs (small molecule drugs and biologics), medical devices and cosmetics, and similar attention to the divisions and affiliated food evaluation center of the State Administration for Market Regulation, which regulates finished food products.
作者: GET    時間: 2025-3-26 17:29
Adverse Drug Events to Biomedicines most prominent role in this area in China are the human genetic resource (HGR) regulations. This chapter examines the development of the area of biosecurity overall, with particular attention to the HGR regulatory regime.
作者: reception    時間: 2025-3-27 00:22
Designing Effective Content Marketing Poststrative and quality control in the special foods area, such as required registrations for infant formula and medical foods. This chapter examines the regulatory landscape for general and special foods (i.e., health foods, infant formula, and medical foods) and their ingredients.
作者: RENIN    時間: 2025-3-27 02:26

作者: Uncultured    時間: 2025-3-27 06:46
2662-141X lso user-friendly for those with no experience.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 analyz
作者: GEM    時間: 2025-3-27 11:19
https://doi.org/10.1007/978-3-642-48906-8ularly in the areas of food and drug safety, and the desire to provide higher quality health and wellness resources to people and to build modern food and health care industries that focus on promoting innovation. This chapter also outlines the further content of the book, which will cover the mechanics of this area of regulation.
作者: 小臼    時間: 2025-3-27 17:27

作者: atopic-rhinitis    時間: 2025-3-27 20:30

作者: 具體    時間: 2025-3-28 00:26

作者: 愚笨    時間: 2025-3-28 02:57
Introduction and Methodology,y. This area of regulation has grown considerably in volume and complexity in the twenty-first century in response to public health challenges, particularly in the areas of food and drug safety, and the desire to provide higher quality health and wellness resources to people and to build modern food
作者: 思想上升    時間: 2025-3-28 08:45

作者: 詞匯表    時間: 2025-3-28 11:05
Administrative Law Concepts and Enforcement Powers,the role that each of these branches play in FDD regulation. It focuses on the administrative law enforcement process that occurs through administrative agencies and through the courts. This chapter discusses the ways in which enforcement begins, the collection of different types of evidence and the
作者: alcohol-abuse    時間: 2025-3-28 14:56

作者: 截斷    時間: 2025-3-28 19:56

作者: faculty    時間: 2025-3-28 23:20
Medical Device Regulation,el of medical technology approved for use in health care in China. It discusses the general procedures and requirements for pre-market approval and risk-based regulation over the life cycle of devices, into the post-market environment. It also examines more specific methods for regulating certain ty
作者: 名字    時間: 2025-3-29 05:28
Biosecurity and FDD Research and Development,ce development in China. China is gradually developing an area of law related to the security and protection against misuse of biotechnology: biosecurity. This area includes human, animal, and plant testing and research, as well as issues of bioterrorism. But the rules that have, to date, played the
作者: 非實體    時間: 2025-3-29 08:08
Food Regulation in China,, a large portion of foods are not subject to pre-market approval. Therefore, the challenges for the government in this area have been unique, including experiments with risk analysis-based regulation and different types of criminal and administrative penalties and measures to achieve better adminis




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