Validation, Verification and Transfer of Analytical Methods
This event qualifies for 12 RAC
Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.
Who will benefit:
- QA Managers and Personnel
- Quality Control
- Method Development
- Analytical Chemists
- Validation Specialists
- Laboratory Managers and Supervisors
- Regulatory Affairs
- Training Departments
- Documentation Departments
- Consultants
Speaker and Presenter Information
Dr. Ludwig Huber
Chief Advisor - Global FDA compliance, Labcompliance- Chairman, presenter and panel discussion member at US-FDA Industry Training sessions and conferences
- Served as team member of PDA's task forces "21 CFR Part 11", of US-FDA internal documents, and of the GAMP® special interest group on Laboratory Systems.
- Presenter of the Year of the Institute for Validation and Technology
- Director and chief editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories.
- Author of the books "Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems"
Relevant Government Agencies
Other Federal Agencies
This event has no exhibitor/sponsor opportunities
When
Mon-Tue, Mar 20-21, 2017, 9:00am - 6:00pm
Where
Hilton Zurich Airport
Hohenbuhlstrasse 10
Opfikon-Glattbrugg, Switzerland CH
Get directions
Website
Click here to visit event website
Organizer
GlobalCompliancePanel
