Learn the specific auditing requirements for the initial supplier/contractor qualification and the tools and knowledge you need to plan these audits. We will also cover what to look for throughout the process and when reviewing key documents and quality systems requirements such as SOPs, Validations, Change controls, and investigations.
Gain in-depth knowledge of what to consider when setting up an audit program within a GDP or GMP environment, specifically about factoring in risk analysis methodologies. In addition to understanding ‘what’ is important, participants will understand precisely ‘why’ this is important, why we must consider the wider risk element and why reducing its overall impact is critical to its success.
Join this webinar to learn from other companies about alternatives ways to acquire information from your suppliers and improve your auditing processes.
In this webinar, you will learn how to decide on whether you should conduct a remote GMP audit and, if yes, how to prepare and execute with success in mind.
Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.
This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.
