theta-waves
发表于 2025-3-23 10:32:06
Erfolgreiche Strategiearbeit im Mittelstand of the articles that are most relevant to overseas pharmaceutical companies, and the major regulations related to drug registration, quality management, and inspection. The corresponding guidances are listed and will be discussed in the corresponding independent chapters.
要求比…更好
发表于 2025-3-23 16:39:43
Erfolgreiche Strategien für E-Commerceese State Council in 2008. In this chapter, we’ll briefly introduce the basic knowledge of the Chinese IPR system, the key regulatory policies, and the differences between China and western countries. We hope this section for Pharmaceutical Patent Protection may help overseas and multinational pharm
Bouquet
发表于 2025-3-23 18:34:51
Unternehmensführung & Controllingt ones for multinational pharmaceutical companies and pharmacy school students to understand. We hope this chapter may help the readers get a basic idea of China’s regulatory environment through the understanding of the CFDA structure and function and its differences from its counterparts in the wes
误传
发表于 2025-3-24 02:05:48
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预示
发表于 2025-3-24 03:00:36
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许可
发表于 2025-3-24 06:41:18
https://doi.org/10.1007/978-3-8350-9511-3ous clinical phases have to follow the CFDA’s defined requirements; the investigator’s responsibilities and safety reporting requirements are very unique from those of the western world; all the clinical sites and investigators have to be certified by the CFDA to conduct the clinical trials; all eth
浸软
发表于 2025-3-24 11:51:23
Ergebnisse der empirischen Untersuchung,ug registration in China, IMCT data shall be in line with the requirements of the CFDA regulations. In this section, we’ll introduce the development strategies with a focus on IMCT, its subtypes, the corresponding advantages and disadvantages of each potential pathway, the application processes, the
尾巴
发表于 2025-3-24 16:28:25
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腐蚀
发表于 2025-3-24 20:15:26
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LEERY
发表于 2025-3-25 02:29:51
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