Making compliance turnkey for elemental impurities testing in pharmaceuticals

With regulatory requirements, validation protocol and data integrity all at the forefront of compliance, it is important to equip the laboratory with more than just analytical equipment. A turnkey solution is to provide analytical chemists with the tools, resources, and knowledge to develop compliant protocols and procedures. During this webinar we will review a total ICP-MS based solution approach for solving elemental impurity testing in pharmaceuticals.

In this webinar, learn about:

• USP Chapters 232 and 233 and ICH Q3D
• 21 CFR Part 11 requirements and compliance
• Solutions to streamlining your ICP-MS based elemental impurity testing
• Software and computer system validation requirements to ensure data integrity and compliance

Who Should Attend (Who will benefit from this webinar?)

• Pharmaceutical chemists and employees
• Lab managers and directors
• API manufacturers
• Excipient manufacturers

Certificate of attendance

All webinar participants can request a certificate of attendance, including a learning outcomes summary for continuing education purposes