使激动
发表于 2025-3-23 10:00:35
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
广大
发表于 2025-3-23 15:34:28
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BIAS
发表于 2025-3-23 21:19:44
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Gum-Disease
发表于 2025-3-24 01:37:30
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babble
发表于 2025-3-24 02:22:27
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
粘连
发表于 2025-3-24 09:09:00
https://doi.org/10.1007/978-3-031-61901-4Chinese Food Law; Chinese Drug Law; Human drugs; Cosmetics; Medical devices; China FDD Regulation; Biosecu
圣人
发表于 2025-3-24 13:43:14
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Negligible
发表于 2025-3-24 18:43:26
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linear
发表于 2025-3-24 20:28:11
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.
FLEET
发表于 2025-3-24 23:38:29
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