How to Satisfy Regulatory Demands for Supplier Qualification & Auditing

Course Overview

Do you find yourself struggling to keep up with the ever-increasing expectations of regulators regarding supplier qualification and auditing in the pharmaceutical industry?

It’s challenging to interpret and implement new guidelines, like the recently updated USP Chapter <1083>, which can be confusing and overwhelming. This can lead to delays, higher costs, and even product recalls or patient harm. It’s essential to ensure that your supplier qualification and auditing practices are robust and compliant to avoid the severe consequences of regulatory scrutiny.

We understand that the consequences of inadequate supplier qualification and auditing practices can be far-reaching, so we’re here to help.

Our upcoming webinar will provide you with the knowledge and tools to confidently navigate the regulatory landscape and achieve compliance. Our expert, Paul Palmer, will guide you through the intricacies of supplier qualification and auditing, focusing specifically on interpreting the new USP Chapter <1083>.

You’ll understand regulatory expectations comprehensively and learn effective organisational implementation strategies.

Don’t let the complex landscape of supplier qualification hold you back. Join us and gain the knowledge you need to succeed.