Share
Process Validation for Manufacturing of Terbinaforce Tablets
Praveen Kumar
(Author)
·
Meenu Chaudhary
(Author)
·
LAP Lambert Academic Publishing
· Paperback
Process Validation for Manufacturing of Terbinaforce Tablets - Kumar, Praveen ; Chaudhary, Meenu
Choose the list to add your product or create one New List
✓ Product added successfully to the Wishlist.
Go to My Wishlists
Origin: U.S.A.
(Import costs included in the price)
It will be shipped from our warehouse between
Friday, August 09 and
Wednesday, August 21.
You will receive it anywhere in United Kingdom between 1 and 3 business days after shipment.
Synopsis "Process Validation for Manufacturing of Terbinaforce Tablets"
SUMMARY- Validation is the way toward building up narrative proof exhibiting that a system, process, or movement did in testing and afterward creation keeps up the coveted level of consistence at all stages. In the pharmaceutical business, it is imperative that notwithstanding last testing and consistence of items, it is additionally guaranteed that the procedure will reliably deliver the normal outcomes. Validation mainly Based on, FDA regulations describing current good manufacturing practice (CGMP) for finished pharmaceuticals are provided in 21 CFR parts 210 and 211.A wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following: - Equipment validation- Facilities validation- HVAC system validation - Process Validation- Analytical method validation- Computer system validation- Packaging validation- Cold chain validation need of Process Validation for Assurance of quality of the product.
- 0% (0)
- 0% (0)
- 0% (0)
- 0% (0)
- 0% (0)
All books in our catalog are Original.
The book is written in English.
The binding of this edition is Paperback.
✓ Producto agregado correctamente al carro, Ir a Pagar.
