Building a Sustainable Validation Program This webinar will teach attendees best practices for building a sustainable validation program. Attendees will learn how to avoid common pitfalls when executing validation protocols. Why Should You Attend: If you are looking for the answer to the following questions, you will certainly benefit from attending this webinar on building a sustainable validation program:
Though company has expertise in process validation it is never quite able to keep up with facility and equipment changes requiring never ending equipment qualification (IQ, OQ, PQ). What is the difference between a validation master plan and a set of validation SOPs. How PLC-based systems or laboratory equipment should fall within the methods validation program, software validation program, or even the equipment qualification program.
Well, the answers to these and many more typical questions are now available in this simple to understand, yet detailed webinar designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable validation program.
Areas Covered in the Webinar:
Define a sustainable structure of a firm’s validation program Understand how change control and other quality programs feed into the validation program
Define minimal recommended tests and verifications for equipment qualification Discuss what FDA is really looking for in process validation Specify the deliverables associated with software validation Common pitfalls to avoid when executing validation protocols How to estimate costs and time associated with validation How to respond to customer and regulatory audit observations associated with validation
Who Will Benefit:
Internal Auditors Regulators Legal Departments Compliance Officers Validation Managers QC Managers QA Managers Facilities and Engineering Department Staff Compliance Consultants Senior Management
For more details please visit our website: http://www.complianceonline.com/ecommerce/control/trainingFocu s/~product_id=703550/~Building_a_Sustainable_Validation_Program ?channel=DOC_organic http://www.complianceonline.com/