1.
Discussion on Drug Batch Number and Expiration Date of Norm Signal and Discriminate
浅谈药品批号和有效期的标示与识别
2.
The shipping mark is inconsistent with the documents; The batch number or quantity of the imported drugs is inconsistent with that in the documents;
装运唛头与单证不符的；进口药品批号或者数量与单证不符的；
3.
This porduct is widely used to shoes print words regarding date of manufacture and batch number etc. in the industries such as foodstuff. everage and pharmaceutical etc.
该产品广泛应用于鞋业、食品、饮料、医药等行业在包装物上打印生产日期、批号等字样。
4.
The druggist put in a full stock of drugs.
那位药商进了一大批药品。
5.
Photocopy of the Drug Import Registration Certificate (or the copy of Pharmaceutical Product Registration Certificate) and photocopy of the Drug Import Approval;
《进口药品注册证》（或者《医药产品注册证》）复印件、《进口药品批件》复印件；
6.
It is normal practice for companies to use a bulk batch number that is different from the finished product batch when the bulk is packaged as several sub-batches.
公司一般的做法是使用一个与成品批号不同的散装批号，然后包装成几个下属批号。
7.
those who import or export psychotropic drugs without authorization.
未经批准擅自进口、出口精神药品的。
8.
Methods on Enforcing GSP for Drug Distributors and Suggestions;
药品批发企业实施GSP的方法和建议
9.
MDCL maintains a record for each Batch of products and identifies the quantity manufactured and released. The Batch record is verified and authorized by the Quality Assurance Manager.
本公司保存每批产品的批号并确认生产及发出数量。由品质经理检验并授权记录批号。
10.
Considerations on Approving Advertisement of Prescription Drug
对处方药药品广告审批问题的几点思考
11.
Influence of“Provisional Regulation on the Approval of Internet Drug Business”on Retail Pharmaceutical Enterprises;
浅析《互联网药品交易服务审批暂行规定》对药品零售企业的影响
12.
Decree No. 6 of the State Food and Drug Administration of the People's Republic of China, Promulgating the Measures for the Administration of Business Licenses of Drugs
国家食品药品监督管理局令第6号,发布《药品经营许可证管理办法》
13.
Direct labor on job No.365 is recorded as follows...
号码为365的产品批次的直接人工会计分录为…
14.
In terms of the biological products within the range of examination, approval and issuance specified by the State Food and Drug Administration,
国家食品药品监督管理局规定批签发的生物制品，
15.
For a biological product within the range of examination, approval and issuance specified by the State Food and Drug Administration
国家食品药品监督管理局规定批签发的生物制品
16.
These records shall be kept for one year after the expiry date of the recorded batch of medicine.
记录保存至该批药品的有效期满后１年；
17.
Improvement of Drug Wholesaler Marketing Management and Regulation of Drug Circulation;
搞好批发企业经营管理 规范药品流通秩序
18.
Analysis on Flawed Project of GSP Certification for Drug Distributors and Corresponding Measures;
药品批发企业GSP认证缺陷项目分析及对策