The test item Chuanbei is one of the traditional Chinese medicinal herbs、 mainly grown in Sichuan、 Yunnan and other places. The main components of Chuanbei include saponins、 mucus、 proteins、 oils、 minerals、 volatile oils、 etc. Therefore、 the quality evaluation of Chuanbei mainly includes the following aspects: 1. Appearance quality: The appearance of Chuanbei should be white or grayish white、 and each part should not show discoloration、 blackening、 decay、 or paste. 2. Odor quality: The odor of Sichuan scallops should have a special and refreshing aroma、 and there should be no musty、 foul、 or sour odor. 3. Content determination: Determine the effective ingredients in Chuanbei、 such as total saponin content、 powder fineness、 moisture content、 etc. 4. Pesticide residues: Detect the pesticide residues in Sichuan scallops to ensure that the products comply with relevant national standards and regulations. 5. Heavy metals and microorganisms: Detect the presence of harmful substances such as heavy metals in Sichuan scallops、 as well as the quantity and type of microorganisms、 to ensure product quality and safety. In summary、 for the quality testing of Sichuan Fritillaria、 a comprehensive quality evaluation and testing should be conducted based on factors such as its growth environment、 picking time、 and drying method. Detection scope: Wild Sichuan scallops: Wild Sichuan scallops collected from wild mountain forests have characteristics such as loose texture、 easy peeling、 rich mucus、 and a fragrant odor due to factors such as growth environment and picking time. Cultivated Chuanbei: Chuanbei is mainly grown in Yunnan、 Sichuan、 Guizhou and other places. Due to factors such as growth environment and picking time、 its quality is inferior to wild Chuanbei、 but it has the advantage of being cheap. Steaming Chuanbei: It is the process of steaming Chuanbei under high temperature and pressure to make it tough and sticky、 which can increase the content of effective ingredients. Drying Chuanbei: It means heating and drying Chuanbei to gradually reduce its moisture content、 making it convenient for long-term storage and use. Relevant reference standards and specifications T/CACM 1020.26-2019 Genuine medicinal materials Part 26: Chuan Beimu T/CACM 1021.32-2018 Chinese medicinal materials Product specification grade Chuan Beimu T/YNZYC 0066-2022 Green medicinal material Chuan Beimu 52 Pharmacopoeia Part 1-2020 Medicinal materials and decoction pieces. The purpose of processing test reports for Chuan Beimu with three pictures is to evaluate the quality of the product; 2. Determine the product quality level、 i.e. the severity of defects; 3. Inspect the process flow and supervise the process quality; 4. Collect、 statistics、 and analyze quality data to lay the foundation for quality improvement and management activities; 5. Introduce arbitration inspection to determine the responsibility for quality accidents. The purpose of handling third-party testing reports is to obtain an independent、 objective、 and professional evaluation result to confirm whether the tested items or services comply with relevant regulatory standards、 quality requirements、 or technical specifications、 and to verify their safety、 reliability、 and performance. Third party testing reports are typically used in areas such as product certification、 market access、 supply chain management、 trade negotiations、 and dispute resolution. Precautions for Testing Report: Carefully read and understand each section after receiving the testing report. Ensure that there is a "research and testing special seal" and official seal in the report、 and check the anti-counterfeiting QR code to confirm its effectiveness. Confirmation information: Verify whether personal or organizational information is accurate and accurate. If the report is not stamped with the "Research and Testing Special Seal" or official seal、 it is invalid. Pay attention to the test results: Focus on the summary and detailed information of the test results. If in doubt、 consult relevant engineers and it is strictly prohibited to alter the report. Pay attention to the reference range: Check the reference range of the test results to see if the results are normal. As the reference range varies depending on factors such as samples、 test methods、 reference standards、 etc.、 please contact our engineers to discuss your specific situation. Objection handling: If you have any objections to the test report、 please file an appeal within 15 days of receiving the report. Late appeals will not be accepted. The above article is a partial list. For more testing needs and details、 please consult the online consultant of the free consulting agency: 18501763637

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