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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.

Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has proposed new approaches chapters for integrated validation, verification and transfer of analytical procedures, for equivalency testing and for statistical evaluation.

Learning Objectives:
Learn about the regulatory background and requirements for validation of analytical methods and procedures
Learn how to plan, execute and document development and validation of methods developed in-house
Be able to explain the different requirements for validation, verification and transfer of analytical procedures
Understand the principles of validating methods developed in-house, verification of compendial methods, transfer of analytical procedures and demonstrating equivalency to compendial methods

Who will Benefit:
QA managers and personnel
Quality control
Method development
Analytical chemists

Note:
Use coupon code 232082 and get 10% off on registration.

For Registration:
http://www.complianceonline.com/lab-analytical-compendial-method-ich-q2-glp-part11-annex11-qbd-workshop-seminar-training-80291SEM-prdsm?channel=eventsinamerica

There may be many networking opportunities at the Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH). Find out more in the event details below.

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Website: http://www.complianceonline.com/lab-analytical-compendial-method-ich-q...
Conference/Event Dates: 08/04/2015 - 08/05/2015
Conference/Event Hours: 8:30 AM to 4:30 PM
Classification: B2B
Primary Industry: Sciences
Other Industries: Business, Sciences
Estimated Attendance: 30
Cost to Attend: One Registration: $1499
Audience: QA managers and personnel
Quality control
Method development
Analytical chemists
Validation specialists
Venue: Grand Hyatt San Francisco
Venue Phone: (415) 398-1234
Venue Type: Indoor - Hotel
Show Owner:ComplianceOnline

Booth Size Booth Cost   Available Amenities
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Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

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