Virtual Seminar on Analytical Method Validation Process

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Category Analytical Method, Validation Process, Project Management, Clinical Lab Science, Information Technology, Validation Planning, Compliance 2017 courses, Analytical Method Validation, Quality by Design

Deadline: November 02, 2017 | Date: November 03, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-09-21 15:13:20 (GMT+9)

Call For Papers - CFP

Use of analytical methods is widespread. However, there are no formally accepted guideline or formats for the overall process of design, development, optimization & validation of analytical methods.

Why should you Attend:

Method validation is the process of demonstrating that analytical procedures are suitable for their intended use and that they support the identity, strength, quality, purity and potency of the drug substances and drug or other products.

Areas Covered in the Session:

Method Development, Optimization and Validation Approaches

Method Validation -High Level

System Suitability

Validation Components

Accuracy

Who Will Benefit:

Anyone in a laboratory setting that needs to validate methods

Analysts

Lab Supervisors and Managers

QA/QC Managers and Personnel

Consultants

Validation Specialists

Chemists

Speaker Profile:

Angela Bazigos Seasoned Executive with 40 years of experience in the Life Sciences & Healthcare Industries. Positions include Chief Compliance Officer http://morflearning.com/angelabazigos/. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Turnarounds and Business Development.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com