青年中文gmp的意思
gmp中文翻譯：
abbr.藥品生產質量管理規范（GoodManufacturingPractice）
All numbering within this section coincides with actual numbering in the GMP Provision.───本節中的所有編號與GMP規定的實際編號一致。
Process validation is a key in execution of GMP in pharmaceutical enterprise.───工藝驗證是制藥企業實施GMP規范的關鍵問題。
These contract laboratories are not subject to routine GMP inspections.───這些合同式實驗室不必接受GMP的例行檢查。
It may not be cost-effective to locate storage tanks as close as possible to the point of use, within high-cost, GMP -finished areas.───在高成本、區域內，盡可能靠近使用點安置貯水罐并不會節約成本。
The productive process is sealed and no dead corner, granulating uniform, easy to clean. It conforms to the requirements of GMP.───生產過程密閉無死角，制粒均勻、清洗方便，完全符合GMP要求。
It would be unrealistic to expect drug product GMP concepts to apply to the production of these progenitors.───使制劑的GMP概念適用于這些物質的生產是不現實的。
Create the GMP self-inspection plan of the company and participate in its implementation.───負責制定公司GMP自檢計劃，并參與組織實施。
The system of quality assurance incorporating GMP and quality control should be fully documented and its effectiveness monitored.───結合GMP和質量控制的質量保證系統應該完全文件化并有效監督。
Hualan is the largest producer of vaccine in Asia with a state of the art facility that operates according to sFDA GMP and EU guidelines.───華蘭是與最先進的設施，國家在亞洲最大的疫苗生產商的操作根據國家藥監局GMP和歐盟的指導方針。
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.
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.
Familiar with quality system requirements of GMP, ISO, FDA and related regulatory.
Responsible for ensuring GMP compliance in production department activities.
A pilot plant complies with GMP has been established for trial production.
Do you establish a well-organized GMP documentation system?
The general circumstances on the conception, quality of GMP and Chinese GMP for radiopharmaceutical manufacturers are introduced briefly.
To file the batch record in the GMP library termly.
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.