This event has ended

GMP Requirements for Validation and Re-Validation of Analytical Procedures

ComplianceOnline

Tuesday, August 6, 2013 from 10:00 AM to 11:00 AM (PDT)

GMP Requirements for Validation and Re-Validation of...

Ticket Information

Ticket Type Remaining Sales End Price Fee Quantity
Single Registration 20 Tickets Ended $249.00 $14.69
Group Registration 20 Tickets Ended $999.00 $39.92

Who's Going

Loading your connections...

Share GMP Requirements for Validation and Re-Validation of Analytical Procedures

Event Details

This webinar will explain the cGMP and ICH validation requirements for analytical procedures and discuss key factors that would affect validation process of analytical procedures. It will review the differences between validation and re-validation plan.

Why Should You Attend:

New medicines are developed every day to meet medical needs and improve quality of life. Analytical procedures are used to establish acceptance criteria and monitor quality of drug products. Therefore, validation becomes a critical process especially with the changes throughout the drug development process. It is important to understand validation requirements set forth by ICH and GMPs.

This webinar will present the common deficiencies in relation to method validation, outline regulatory requirements and the change control process needed to stay in compliance.

Learning Objectives:

Upon completion of this session, attendees will understand cGMP and ICH validation requirements for analytical procedures and learn key factors that would affect validation process of analytical procedures. It would help scientists to develop process to evaluation method validation, review changes, and determine when re-validation would need to take place. It will discuss observations and infractions related to method validation.

Areas Covered in the Webinar:

  • Deficiencies related to Method Validation.
  • Factors affecting Quality of Medicines.
  • Validation Characteristics
  • Validation vs Re-Validation plan
  • Tracking record of validation project.
  • Change control of validation

Who will Benefit:

  • Senior management in pharmaceutical analysis
  • Pharmaceutical scientists
  • Analysts and lab managers
  • QA managers and personnel
  • Regulatory affairs
  • Contract research laboratories


For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703041?channel=Eventbrite

Have questions about GMP Requirements for Validation and Re-Validation of Analytical Procedures? Contact ComplianceOnline

When

Tuesday, August 6, 2013 from 10:00 AM to 11:00 AM (PDT)


  Add to my calendar

Organizer

ComplianceOnline

At ComplianceOnline, we are focused on :

 

  • Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.
  • Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.
  • Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.
  • Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

 

 

 

  Contact the Organizer

Please log in or sign up

In order to purchase these tickets in installments, you'll need an Eventbrite account. Log in or sign up for a free account to continue.