Data Integrity for Elemental Analysis: From Raw Sample to Results

Pharmaceutical laboratories conducting elemental analyses – whether for small molecule or biopharmaceutical applications – must ensure reliable results, guaranteeing data integrity throughout their workflows, from raw sample to final results. In this webinar, you will learn about key considerations around sample preparation, analytical methodology, and all the system validation considerations that go along with it.

Register free: https://www.chromatographyonline.com/lcgc/results

Event Overview:

In the highly regulated pharmaceutical industry, data integrity is critical. Pharmaceutical laboratories conducting elemental analyses – whether for small molecule or biopharmaceutical applications – must ensure reliable results, guaranteeing data integrity throughout their workflows, from raw sample to final results. Software that helps your labs comply with the stringent 21 CFR Part 11 regulations is crucial, along with system qualification and computer system validation. In this webinar, you will learn about key considerations around sample preparation, analytical methodology, and all the system validation considerations that go along with it.

Key Learning Objectives:

• Understand laboratory requirements for elemental impurity testing
• Learn how to develop and validate sample preparation for elemental impurity testing
• Explore analytical considerations with regard to instrument and validation requirements

Who Should Attend:

• Managers, directors and chemists/technicians of pharmaceutical and nutraceutical QA/QC labs
• Managers, directors and chemists/technicians of biopharmaceutical labs

Speakers

Pat Doherty
Senior Account Manager
PerkinElmer

Pat Doherty is a Senior Account Manager at PerkinElmer. He holds a B.Sc. (Hons) in analytical chemistry, M.Sc., in Advanced Analytical Techniques with Research & Quality Management and a PG. Dip in Biopharmaceutical Analytical Techniques. Based in Ireland, the largest producer of pharma products in the EU and host to almost every global pharma company, Pat interacts with the Pharma industry on a daily basis in areas including selecting the appropriate analytical instrument for end-user requirements, creation of URS, IQ/OQ protocols, 21 CFR 11/Eudralex compliance and protocols for compliance with the testing requirements of USP, EP, JP ChP etc.


Sandeep Kumar
Field Application Scientist
AmericasPerkinElmer, Inc.

Sandeep Kumar is currently a Field Application Scientist at PerkinElmer, specializing in Atomic Spectroscopy. Prior to joining PerkinElmer, he worked in the pharmaceutical industry for more than 13 years and was extensively involved in implementing USP 232/233 in R & D and Production departments. Sandeep is an analytical and physical chemist and specializes in ICP-MS and ICP-OES with extensive knowledge of method development/validation. Sandeep has completed his Ph.D. from Albert Ludwigs University, Freiburg, Germany.

Register free: https://www.chromatographyonline.com/lcgc/results