The implementation of Good Manufacturing Practices (GMPs) is essential for maintaining product quality and ensuring regulatory compliance in industries such as Pharmaceuticals, Cosmetics, and Food. High Performance Liquid Chromatography (HPLC) is a powerful analytical technique that plays a critical role in these industries, offering unmatched sensitivity, selectivity, accuracy, and reproducibility in the quantitation of analytes.
This half-day webinar is designed to provide a comprehensive understanding of how HPLC can be effectively employed in GMP-compliant analytical testing. Participants will learn about the key components of an HPLC system, best practices for system suitability, and the intricacies of mobile phase preparation, column selection, and sample preparation. The course will also cover the importance of proper GMP documentation in HPLC testing and provide an overview of Empower 3 software. By the end of this session, attendees will be equipped with the knowledge and skills to perform GMP analytical testing by HPLC, ensuring the safety, identity, strength, purity, and quality of products in today’s highly regulated industries.
This half-day webinar is ideal for professionals with beginner to intermediate knowledge of GMP analytical testing using HPLC, particularly those working in the Pharmaceutical, Cosmetic, Food, or related industries. It is especially valuable for individuals in Quality Control Laboratories, Analytical Research and Development Laboratories, and Quality Assurance departments.
This workshop covers the following topics:
Fundamental Understanding of HPLC
Gain a clear understanding of HPLC principles, system components, and their importance in GMP analytical testing.
Executing GMP-Compliant HPLC TestingLearn about key HPLC tests while ensuring compliance with GMP documentation requirements.
Effective Use of Empower 3 SoftwareDevelop the ability to use Empower 3 software for managing HPLC data in a GMP environment.
Identifying and Resolving HPLC ChallengesLearn about troubleshooting and how to optimize peak integration and other common issues in HPLC testing.
All participants will receive a certificate of attendance upon completion of the workshop.
Note: Registration closes one week prior to the start of workshop.
Pharma, Cannabis
Kevin has over 25 years of pharmaceutical industry experience working for Novopharm Ltd. and Teva Canada Ltd. For 19 years, he was a supervisor in the following areas: Analytical Research and Development Stability, Quality Control Finished Product, Quality Control Stability, Quality Control Method Transfer, and Operational Excellence. Kevin is known as a positive person with an ability to motivate and guide people to reach their potential. He has demonstrated expertise in compliance, data integrity, laboratory investigations, root cause problem solving, recommending and implementing corrective and preventative actions (CAPAs), and continuous improvement of documentation and efficiency. Kevin graduated from the University of Western Ontario with a M.Sc. in chemistry and has a yellow belt in Operational Excellence. In his spare time, Kevin enjoys long distance running.
