In 22, the new test center of Pharmaceutical Professional Knowledge I for licensed pharmacists: the quality of common drugs.

In p>22, the examination book of Pharmaceutical Professional Knowledge I for licensed pharmacists has changed a lot, and there are some new knowledge points that you may not have known before. Global Ivy Licensed Pharmacist Channel brings "New Test Site of Pharmacy Professional Knowledge I for Licensed Pharmacists in 22: Drug Quality Research" to help you learn this new test site.

Related recommendation: Interpretation summary of the new contents of the test center of Pharmaceutical Professional Knowledge I for licensed pharmacists in 22

The test time for licensed pharmacists in 22 will be October 24th and 25th, and the textbook of Pharmaceutical Professional Knowledge I for licensed pharmacists in 22 has changed a lot, with corresponding test centers added in each chapter.

Tips: Global Ivy provides free appointment SMS reminder service, and we will inform you by SMS when all regions will register for the 22 licensed pharmacist exam. Welcome to use it!

in p>22, the number of test sites for licensed pharmacists "Pharmaceutical Professional Knowledge I" will be increased:? Drug quality research

Quality research structure confirmation, analysis method establishment and verification, stability inspection drug characteristics inspection guiding principles drug crystal research and crystal quality control guiding principles and drug moisture absorption test guiding principles drug impurity analysis guiding principles impurity classification and impurity inspection items injection safety inspection method abnormal toxicity, bacterial endotoxin (or pyrogen), antihypertensive substances (including histamine substances), allergic reaction, The quality consistency evaluation of generic drugs includes safety evaluation (impurity spectrum of drugs) and effectiveness evaluation (bioequivalence of human body, that is, consistency evaluation of bioavailability). Research on drug crystal form and impurity pattern: the type and purity of polymorph, comparative study, to ensure the correct drug impurity pattern research. To evaluate the dissolution consistency of test preparations and reference preparations in different dissolution media, at least three kinds should be selected besides water. Comparison of Similarity of Dissolution Curves of Medium with pH1.2, 4.5, 6. and 6.8 is recommended for enteric-coated preparations. Similarity Factor (f2) Method in Model-independent Method Human Bioequivalence Test. After single or multiple administration of the same dose of the test drug under similar experimental conditions, the differences between the absorption rate and absorption degree of the drug in the test preparation and the reference preparation are in acceptable order: pharmacokinetic study (evaluation indexes Cmax and AUC), pharmacodynamic study, clinical study and so on. In 22, the number of test sites for licensed pharmacists "Pharmaceutical Professional Knowledge I" was added:? Drug quality research? Upload it as a document to the data download page, and click here to download it for free. In addition, there are more exam outlines for licensed pharmacists in 22, changes in teaching materials, simulated test questions in various subjects, and analysis of real questions over the years. You can download them for free by clicking the button below.