Over three full days hear from FDA, MHRA, and pharmaceutical industry experts as they set the framework for discussion on basic quality systems as well as the influence of ICH Q10 on the industry as a whole. As companies continue to address issues such as data integrity, the quality systems platform of ICH Q10 becomes increasingly important to understand and embrace. The 2018 ISPE Pharmaceutical Manufacturing Conference will examine common issues and address how companies can reach a quality maturity level and use knowledge and process understanding throughout the lifecycle of the product.

Come visit Novatek at Table #7 to learn more about our Quality Management Solutions and how our systems also address data integrity.

Other Learning Objectives:

1. Learn how to avoid the regulatory challenges by assuring accurate, reliable, complete information in drug product application submissions
2. Gain an understanding how to apply key ICH Q10 Principals
3. Learn the do’s and don’ts in every stage of process verification (process design, process qualification, and continued verification