Process Validation for Manufacturing of Terbinaforce Tablets

Name: Process Validation for Manufacturing of Terbinaforce Tablets
SKU: 33974562
Price: 102.99 AUD
Availability: InStock

By:

Format:

Paperback / softback

Show Hide Adult Content

$102.99

Available from supplier

Usually ships in 3-4 weeks

0 in Trolley

Price Match

Wrap this item as a gift ($5.90) - add a free gift card on the next page

Buy Now, Pay Later with:

4 payments of $25.75 with Afterpay Learn more

Availability

Delivering to:

Estimated arrival:

Around 28 Jun - 10 Jul using International Courier

Description

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.

Release date Australia

May 5th, 2020

Author

Audience

General (US: Trade)

Pages

Dimensions

152x229x4

ISBN-13

9786202553414

Product ID

33974562

Customer reviews

Nobody has reviewed this product yet. You could be the first!

Write a Review

Marketplace listings

There are no Marketplace listings available for this product currently.
Already own it? Create a free listing and pay just 9% commission when it sells!

Sell Yours Here