北方药学
北方藥學
북방약학
JOURNAL OF NORTH PHARMACY
2015年
4期
142-142,143
,共2页
进口药品%再注册%受理
進口藥品%再註冊%受理
진구약품%재주책%수리
Import Drug%Re-registration%Acceptance
目的:进一步明确进口药品再注册申请的受理要求。方法:根据相关规定,结合笔者工作经验,归纳总结进口药品再注册申请中的常见问题及解决方法。结果与结论:从一致性、规范性、完整性及有效性等方面提高进口药品再注册的申报资料质量,提高申报效率。
目的:進一步明確進口藥品再註冊申請的受理要求。方法:根據相關規定,結閤筆者工作經驗,歸納總結進口藥品再註冊申請中的常見問題及解決方法。結果與結論:從一緻性、規範性、完整性及有效性等方麵提高進口藥品再註冊的申報資料質量,提高申報效率。
목적:진일보명학진구약품재주책신청적수리요구。방법:근거상관규정,결합필자공작경험,귀납총결진구약품재주책신청중적상견문제급해결방법。결과여결론:종일치성、규범성、완정성급유효성등방면제고진구약품재주책적신보자료질량,제고신보효솔。
Objective:Further defined for import drug re-registration acceptance requirements.Method: In accordance with the relevant provisions, work experience, the author summarized for import drug re-registration of common problems and solutions.Result and Conclusion:From the aspects of consistency, the standardization, integrity and effectiveness of improve the quality of import drug re-registration, improve efficiency.