Test Method Validation - The Characteristics- Webinar By GlobalCompliancePanel

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Category Governance Documents, Compliance, Compliance Training, Compliance Webinar, FDA, ISO, Clinical Trials, risk management, Risk Assessment, management process, Risk Identification, risk management plan, Risk Manager, risk management strategies, quality guidelines, Pharmaceutical Technology Europe, risk management, FDA Inspections, Regulatory Environment, pharmaceutical manufacturing, corporate governance, Good corporate governance, corporate governance principles, Audit Committee, Governance Framework,

Deadline: May 19, 2011 | Date: May 19, 2011

Venue/Country: Wilmington, U.S.A

Updated: 2011-04-25 17:54:33 (GMT+9)

Call For Papers - CFP

Both USP <1225> and ICH Q2 classify test methods employed in the industry into types, based on the intended use and identify the characteristics that must be considered in the validation of each type of method.

In order to perform effective test method validations, the analyst must understand the importance of clearly identifying and understanding the intended use of the test method. With the understanding of the intended use, the analyst will categorize the test method into one of the types identified in the USP and ICH Q2. Based on the type of test method and using the guidance in the USP and ICH Q2 the analyst will identify the characteristics that must be considered for effective method validation.

For each characteristic, the USP and ICH Q2 recommend the experiments that the analyst should performed to demonstrate that the method performs as intended.

Why you should attend: The US FDA and other regulatory agencies are critically reviewing test method validations. Observations like: "Failure to establish accuracy, sensitivity, specificity, and reproducibility of test methods employed by your firm", which appear in Warning Letters and 483 observations demonstrate a complete lack of understanding of the regulatory expectations. Other observations that citing to the individual characteristics demonstrate a lack of appreciation for the contributions of the individual method characteristics on adequate method validations. In order to adequately validate test methods, firms must understand the basic terminology associated with test method validation. This webinar will provide an understanding of:

The types of test methods established by the USP and ICH Q2.

Assay

Identification

Testing for impurities ? quantitative

Testing for impurities ? limit

Performance

The characteristics of test methods as defined in the USP and ICH Q2.

Specificity

Accuracy

Precision

Linearity

Range

Limit of Accuracy

Limit of Detection

How the characteristics apply to the types of methods described in USP and ICH Q2.

The basics of how to experimentally evaluate the characteristics.

Areas Covered in the Session:

The requirement for test method validation

The intended use of the test method

Guidance documents covering test method validation

Types of test methods

Characteristics of test methods

Demonstrating the characteristics

Who will benefit: The following individuals or disciplines will benefit from attending this Webinar:

Quality Assurance personnel

Quality Control Managers

Quality Control Supervisors

Quality Control Analysts

Method development Managers

Method development Supervisors

Method Development Analysts

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00