GMP aspects in practice: Basics for the compilation of a validation master plan

被引:0
|
作者
Oechslein, C [1 ]
机构
[1] Novartis Pharma AG, CH-4002 Basel, Switzerland
来源
PHARMAZEUTISCHE INDUSTRIE | 2004年 / 66卷 / 06期
关键词
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
引用
收藏
页码:769 / 770
页数:2
相关论文
共 50 条
  • [1] GMP aspects in practice: Wipe test for sampling in cleaning validation
    Borchert, D
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2004, 66 (01): : 104 - 105
  • [2] Master planning and validation - Part I: Anatomy of a validation master plan
    Agalloco, J
    Sofer, G
    [J]. BIOPHARM-THE APPLIED TECHNOLOGIES OF BIOPHARMACEUTICAL DEVELOPMENT, 2000, 13 (03): : 40 - +
  • [3] Gulf Regional Sediment Management Master Plan: Case Study Compilation
    Byrnes, Mark R.
    Berlinghoff, Jennifer L.
    [J]. JOURNAL OF COASTAL RESEARCH, 2012, : 72 - 124
  • [4] GMP aspects in practice: GMP conforming design of (CIP) installations
    Kamm, T
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2004, 66 (12): : 1529 - 1530
  • [5] Collaborative Planning in Practice: The Nicosia Master Plan
    Abu-Orf, Hazem
    [J]. PLANNING PRACTICE AND RESEARCH, 2005, 20 (01): : 41 - 58
  • [6] GMP-aspects in practice: Methods for purification
    Borchert, D
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2006, 68 (05): : 613 - 616
  • [7] GMP aspects in practice: Material and manpower flow
    Schwarzat, U
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2005, 67 (09): : 1071 - 1072
  • [8] GMP-aspects in practice:: Calibration in laboratories
    Künzle, J
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2006, 68 (03): : 337 - 339
  • [9] GMP-Aspects in practice: Complaints and recall
    Prinz, H
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2005, 67 (11): : 1327 - 1329
  • [10] GMP aspects in practice:: Handling of laboratory reagents
    Künzle, J
    [J]. PHARMAZEUTISCHE INDUSTRIE, 2004, 66 (05): : 573 - 574