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行业指南:年度产品回顾(香港卫生署药物办公室)
http://www.drugoffice.gov.hk/eps/do/en/doc/guidelines_forms/Guidance%20for%20industry_PQR_201312.pdf?v=d9754u9dx6r
Contents
1. Introduction.............................................................................................................................. 3
2. Purpose of this document ......................................................................................................... 3
3. Scope ........................................................................................................................................ 3
4. Scheduling product quality reviews ......................................................................................... 3
5. Grouping Products .................................................................................................................... 4
6. Preparing product quality reviews ........................................................................................... 4
7. Conducting and documenting a PQR ........................................................................................ 5
8. Evaluating PQR results ............................................................................................................. 7
9. PQR responsibilities with contract manufacturing................................................................... 8
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