Under Analytical Method Validation
Tuition: $150.00  

Instructor: NetZealous001

Duration: 1 Hour(s)
Registration Expiration: 1 day(s)

Code: sm_uamv

Average Student Review: No Reviews

Overview: All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more. Why should you Attend: Any laboratory that supports products for sale or use in the United States must follow Good Laboratory Practices (GLP), a comprehensive system that guarantees validity of results. If you work in pharmaceuticals, chemicals and petrochemicals, and environmental analyses then you are mandated to be following GLP. One of the major tasks in GLP is validation of an analytical method. Areas Covered in the Session: Method Validation The Criteria for a Method Statistical Requirements Maintaining Compliance Who Will Benefit: Analysts Lab Supervisors and Managers QA Managers and Personnel Consultants Validation Specialists Chemists Speaker Profile: John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers on liquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry. Event Cost & Details: One Dial-in One Attendee Price: US$150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com

Key Concepts:
Lab Supervisors, QA Managers

Course Appears in these Categories:
Environmental, Safety and Health, and Transportation

Courses you might be interested in:
HIPPA - Privacy Training
Office Safety/The Safety Secret
Combination Products 2017
Cyber Attacks, Beyond Disaster Recovery - 2017
Effective Supplier Qualification Program - 2017
Achieving Compliance Excellence - 2017
Validation Program to a Building from Top to Bottom - 2017
FDA Inspection and Respond to 483 & How to Prepare them - 2017
CAPA within a Device Quality System - 2017
Environmental Monitoring Program at FDA Regulations - 2017
Laboratory-Developed Tests - Medical devices 2017