GMP造句
(1) Responsible for ensuring GMP compliance in production department activities.
(2) Do you establish a well-organized GMP documentation system?
(3) To file the batch record in the GMP library termly.
(4) A full general GMP inspection is carried out in each year. In addition, inspections for parts of GMP system will be carried out every month.
(5) Germany GMP Architectural Firm enjoys high reputation in Europe and World, ranking No. 1 in Germany. Among Top hundred architectural firms, GMP ranks the fifth place.
(6) Second, We also perform GMP quality system on additive; the behavior is the first executant in this industry, to keep the stable quality of product.
(7) Familiar with quality system requirements of GMP, ISO, FDA and related regulatory.
(8) A pilot plant complies with GMP has been established for trial production.
(9) The general circumstances on the conception, quality of GMP and Chinese GMP for radiopharmaceutical manufacturers are introduced briefly.
(10) Responsible for renewing of production license, GMP certificate etc. according to regulations.
(11) Which hastens the execution of GMP standard and prompts the development of Chinese pharmaceutic machine manufacture.
(12) Laboratory, clean room, control room, datarooom, hospital, GMP drug factory , food factory , electronic factory, textile factory.
(13) Manufactured in the U.S. by a GMP - certified facility; guaranteed quality and potency.
(14) Based on GMP norm, the requirements for the equipment used in axenic raw drug production were discussed in this article.
(15) Effects of cytochalasin B and thawing program on glass micropipette (GMP) vitrification of mouse mature oocytes were investigated.
(16) This article summarised the different aspects of GMP construction of axenic workshop in animal powdery agent and put forward some suggestions.
(17) The machine for food and medicine should be up to the standard of GMP.
(18) Production center is located in the National Biological Industry Base in Guangzhou Science City , providing professional standard GMP production.
(19) NSF conducted a plant audit to verify compliance with GMP and will conduct periodic audits at USANA's facility to ensure continued conformance.
(20) Ensure Production batch record are properly completed according to GMP documentation requirements.
(21) This is normally done by auditing the API manufacturer for GMP compliance, and periodically testing the product to verify the information in the Certificate of Analysis.
(22) Our company produce various antivirotic materials which are all up to GMP standard.
(23) Draft out production management document batch production record, modify process procedure GMP relative record, assure production work has regulation to follow.
(24) Based on the directives of 8-year programme of the general medicine bureau of China, all the pharmaceutical enterprises of China must accord with the demands of GMP by the end of 2000.
(25) WB _ ( 852 ) showed no effect on cAMP andc GMP levels in EAC cells.
(26) The facilities have the advantages such as high efficiency and simple operating, In the tank is equipped with CIP automaticturning cleaning head tonsure a complete cleaning in accordance with GMP.
(27) Responsible for other GSP relevant issues in trading function and GMP execution matters in Development lab.
(28) The appraise committee agree on that the project in the highest flight of China pharmacy industry on MIS based GMP, which is worth being popularized in pharmacy industry.
(29) High - pressure steam sterilizer is the equipment required to be verified in GMP authentication.
(30) Conduct to prepare and modify SOPs, Method Validation Protocol and Report, GMP Documents, etc.
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