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.
In this webinar, you will gain a thorough background in all the important regulatory changes and updates that are going on right now. This will allow you to make informed choices about what regulations impact your operations and need- to- have specific regulatory actions, operational changes, and QMS updates.
This webinar gives you the tips and common mistakes you need to consider to get a world-class and airtight life science supply chain in place.
Gain insights into why upgrading your equipment offer greater security and enhancements to anti-counterfeiting measures, as well as some improvements in operational efficiencies.
In this webinar, you’ll learn about Product Inspection solutions that can increase quality assurance and make compliance easier.
Exciperience is the new virtual event around every aspect of pharmaceutical excipients. It covers all areas from research and formulation to manufacturing and regulatory.
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.
