Your Partner for Regulatory Compliance With Over 25 Years of Experience
Consult With a Validation Expert

Webinar Details

February 26th, 2014
01:00 PM - 02:00 PM EST

The FDA has made significant progress in implementing the concepts of "Quality by Design" (QbD) into pre-market processes. The QbD concept is that quality should be built into a product through a deep understanding of the product, both how it's developed and how it's manufactured. A comprehensive understanding of the risks involved in manufacturing a product and how best to mitigate those risks is also required.

The QbD initiative attempts to provide guidance on pharmaceutical development to facilitate design of products and processes with maximum efficacy, safety profile and product manufacturability. QbD forms the basis of process validation activities conducted by pharmaceutical manufacturers in validating their product manufacturing processes.

Register for our complimentary webinar for a review of "Quality by Design" concepts and a discussion on its relevance to process validation. During our discussion we will have an opportunity to see a demonstration of Validator, a software product that facilitates the adherence to the QbD principles and best practices in process validation.

Registration URL 


Newsletter Sign Up

Sign up for the Compliance Associates Newsletter to stay on top of industry trends, learn about important events, and get answers to your most frequently asked compliance and validation questions.

I understand and agree that registration on or use of this site constitutes to its Privacy Policy.


Our Video

Request More Info

Please select the Circle and click the Submit button.