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Virtual Seminar on Analytical Method Validation Process


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Who should attend?

QA/QC Managers and Personnel Consultants Validation Specialists Chemists

Details

Overview:  
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: support@compliance4All.com

Prices

One Dial-in One Attendee Price: US$290.00

Contact

Event Manager
support@compliance4all.com

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