Validation and Verification of Analytical Methods Professional Training – Coming Soon
By Jenny Sverdlova B.Sc. & Rivka Goldik, D.Sc.
2
Quality Assurance
Pre Clinical Studies
Starts at: 09:30
Duration: 1 Session
Language: Hebrew
Validation and Verification of Analytical Methods Professional Training
Master the critical regulatory requirements and technical expertise essential for analytical method validation in pharmaceutical manufacturing. This comprehensive one-day seminar provides regulatory professionals with practical knowledge of ICH Q2/Q7 guidelines, pharmacopeia standards, and validation parameters across all test categories.
Key Learning Outcomes:
- Navigate ICH Q2 and Q7 regulatory frameworks with confidence
- Apply USP chapters <1224>, <1225>, and <1226> requirements effectively
- Execute validation protocols for identification, assay, impurities, dissolution, and biological methods
- Implement robust validation strategies that withstand regulatory scrutiny
Target Audience:
QA/QC professionals, analytical chemists, and quality managers requiring current expertise in method validation compliance.When: Soon
Gstudy Training Center HaifaAbout Jenny Sverdlova B.Sc.
Jenny Sverdlova - Quality and Laboratory Expert Over 15 years of pharmaceutical quality experience across analytical laboratories, quality assurance, and regulatory compliance. Expert in laboratory investigations, audit management, and quality system implementation. Education: B.Sc. Chemistry, Ben Gurion UniversityAbout Rivka Goldik, D.Sc.
A DSc graduate of the Faculty of Chemistry at the Technion and B.Sc. in education of chemistry at the Faculty of Education in Science and Technology at the Technion – Israel Institute of Technology, Haifa, Israel.During her studies she was also involved in laboratory training and teaching analytical chemistry.Dr. Goldik began in the pharmaceutical industry in 1996 and has served...
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Master the critical regulatory requirements and technical expertise essential for analytical method validation in pharmaceutical manufacturing. This comprehensive one-day seminar provides regulatory professionals with practical knowledge of ICH Q2/Q7 guidelines, pharmacopeia standards, and validation parameters across all test categories.
Registration Information
Contact: Gstudy@gsap.co.il