Validating pharmaceutical systems : good computer practice in life science manufacturing
tarafından
 
Andrews, John.

Başlık
Validating pharmaceutical systems : good computer practice in life science manufacturing

Yazar
Andrews, John.

ISBN
9780203500439
 
9781135487942
 
9781135487980

Fiziksel Tanımlama
1 online resource (xix, 549 pages)

İçerik
chapter 1 Considerations for Computerized System -- chapter 2 An Inspector's Viewpoint -- chapter 3 State-of-the-Art Risk Assessment and -- chapter 4 Validation Planning and Reporting -- chapter 5 Supplier Audits: Questions and Answers -- chapter 6 Developing Good Specifications -- chapter 7 Traceability of Requirements Throughout the -- chapter 8 Good Documentation in Practice -- chapter 9 Good Testing Practice: Part 1 -- chapter 10 Enterprise Resource Planning Systems -- chapter 11 Calibration in Practice -- chapter 12 Validating Legacy Systems -- chapter 13 Technology Transfer Keys -- chapter 14 Qualifying SCADA Systems in Practice -- chapter 15 The Application of GAMP 4 Guidelines to -- chapter 16 The Validation of a LIMS System�A Case -- chapter 17 Compliance and Validation in Central and -- chapter 18 Distribution Management Validation in -- chapter 19 Good Testing Practice: Part 2 -- chapter 20 Practical Applications of GAMP Version 4.

Konu Terimleri
Pharmaceutical technology -- Data processing.
 
Pharmaceutical industry -- Data processing.

Yazar Ek Girişi
Andrews, John.

Elektronik Erişim
Click here to view.


KütüphaneMateryal TürüDemirbaş NumarasıYer Numarası[[missing key: search.ChildField.HOLDING]]Durumu/İade Tarihi
Çevrimiçi KütüphaneE-Kitap540260-1001RS122.2 .V35 2005CRC E-Books