Potdar manohar a (9 Ergebnisse)

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Hardcover. Zustand: As New. 2nd Edition. Contents Foreword. Preface. Acknowledgements. List of abbreviations. Introduction. Part I 1. Regulatory requirements for pharmaceutical plants. 2. Project management. 3. Pharmaceutical validation. Part II 4. Pharmaceutical facility design. 5. Support Serv 266 pp.…

Zustand: New. In English.

Zustand: New. In English.

Soft cover. Zustand: As New. Contents Foreword. Preface. Acknowledgements. Introduction. 1. Personnel. 2. Surroundings buildings and facilities. 3. Equipment. 4. Materials management. 5. Quality management. 6. Manufacturing operations and control. 7. Documentation and records. 8. Pharmaceutical validation. 9. Outsourcing. 10. Post operational activities. 11. Sterile pharmaceutical products. 12. Site and plant security. 13. Safety and environmental protection. 14. Good pharmaceutical wholesaling practices. 15. Pharmaceutical audit. Glossary. Bibliography. Index. Indian Pharmaceutical Industry is becoming global at high pace. This resulted in high pressure on the industry for quality products and practices. Thus cGMP has acclaimed key position. Practicing cGMP requires clear understanding at conceptual and implementation level and that too at shop floor and middle management level. This book is written in simple and easy to implement manner. Salient features All current issues of cGMP demanded by regulatory authorities like W.H.O. M.H.R.A. T.G.A. U.S.F.D.A. and also Indian F.D.A. are fully discussed profusely referenced and thoroughly illustrated in simple and easy to understand language. Covers other important topics like plant site security environmental issues distribution of products and preparing for the regulatory audits etc. 798 pp.…

Zustand: New. In English.

Zustand: New. In English.

Zustand: New. In English.

Zustand: New. In English.