Licensed pharmacists and licensed western pharmacists have the same contents and materials in the examination of pharmaceutical affairs management and laws and regulations.
However, both Chinese pharmacists and western pharmacists need to apply for this subject, which is not universal. If they passed the Chinese pharmacist exam last year and take the western pharmacist exam this year, they need to apply again.
The laws and regulations on Chinese medicine and western medicine examinations have the same content. The first method has *** 1 1 chapter, which can be reviewed in three parts.
The first part: First, learn the four stages of research and development, production, management and use of drugs in the whole life cycle, namely chapter 4 and chapter 5, of which chapter 5 scored the highest in the exam. The research focuses on the licensing system and GCP, GMP and GSP.
The second part: Learn the national requirements for the management of traditional Chinese medicine, specially managed drugs, medical devices, health food and cosmetics, drug advertisements, and the management of drug-related personnel (licensed pharmacists), with a total of 1, 6, 7, 9, 1 1 chapters, of which the seventh chapter is the key chapter of the examination, and the drug, hemp and sperm have been tested over the years. Chapter 6 is about the examination scores of Chinese medicine, which may be improved. The summary is about the management of Chinese herbal medicines, Chinese herbal pieces and Chinese patent medicines; Chapters 1, 9, 1 1 are relatively simple, and you can score if you understand them.
Part III: Understand the drug system implemented by the state and relevant administrative departments and the responsibilities for violating the drug safety law, namely, Chapter II, Chapter III, Chapter VIII and Chapter 10. 10 chapter content test high score. During the review, we will focus on the identification of counterfeit and inferior drugs and the administrative and criminal responsibilities for the production, sale and use of counterfeit and inferior drugs. The second chapter focuses on reviewing the national essential drug system. The third chapter focuses on the division of responsibilities of various departments. Chapter 8 focuses on the management of drug instructions and labels.