The ongoing company is compiling trial reports and has entered the last stage of its clinical trial. The Company will apply for the SFDA final approval of this product when the Assessment Data are prepared. Related StoriesStudy shows surgery may not be a best option for AC joint dislocationsExcessive OR traffic during surgeries leads to postoperative infectionsU.S 2nd Annual Obesity Summit: 35 main U.S. Health societies see how they are able to treat obesity’The successful taking in of 63 clinical check cases that were carried out at SFDA appointed hospitals is definitely a milestone in our company’s history. It symbolizes the acceptance of our technology by hospitals and doctors, and the acknowledgement and acceptance of our item by patients. We will commence production and advertising of our item as as we receive SFDA approval soon,’ stated Ms Hui Wang, CEO of Advanced BioMedical Technologies Inc.We combined results first within ancestry groups and across ancestry groups, using fixed-effects meta-analyses. We next tested for an association between protein-inactivating mutations in NPC1L1 and the risk of coronary heart disease. In each scholarly study, we estimated the chances ratio for disease among carriers of any NPC1L1 inactivating mutation, as compared with noncarriers. A P value of less than 0.05 was considered to indicate statistical significance. The R computer software was used for all analyses. Outcomes Rare Inactivating Mutations in NPC1L1 After sequencing NPC1L1 in 7364 patients with coronary heart disease and in 14,728 controls without such disease, we identified 15 mutations that were expected to inactivate NPC1L1 .