Webinar Pack
Pack of FIVE: Best Selling Lab Related Webinars by GlobalCompliancePanel Actual Price:
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GMP Expectations for Products Used in Early Phase IND Studies FDA issued a guidance document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition
Instructors:
to those that cover the CMC sections for IND submissions at Phase 1.
Dr. Ludwig Huber Chief Advisor - Global FDA compliance, Agilent Technologies
Understanding Analytical Test Results: Comparing Two Sets of Data The class will cover the understanding the properties of single test results and how they may be compared.
Ludwig Huber, Ph.D., is Director of Labcompliance and Chief Advisor for global FDA compliance at Agilent Technologies. ..more
There are many problems that arise from a misunderstanding of the properties of single data sets and the problems are compounded when data sets are compared.
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory.
Steven S Kuwahara Founder & Principal, GXP Biotechnology, LLC Steven S. Kuwahara, Ph.D. is the founder and Principal of GXP BioTechnology LLC, a consulting firm that works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals. ..more
Validation of Analytical Methods and Procedures Analytical methods should be validated to ensure reliability, consistency and accuracy of analytical data. Method validation has been a requirement of FDA and international regulations and accreditation standards such as ISO 17025 since many years.
Richard Poser President, First Quality Inc
Richard Poser, PhD is President of First Quality Inc., a quality consulting firm focused on Quality Systems, Training and Validation. ..more
Risk-Based Validation of cGMP Systems This presentation will review a methodology for implementing RiskBased Validation of test equipment, facilities and analytical instruments used in GLP, cGMP and GCP facilities.
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About GlobalCompliancePanel GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online compliance training by creating a single window of learning opportunities for compliance professionals & providing a forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning and development on/through our website. Keep track of all webinars arranged for your industry through notifications & event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for professionals. GlobalCompliancePanel www.globalcompliancepanel.com 1000 N West Street Suite, 1200 Wilmington DE 19801 Phone: 800-447-9407 or Fax your PO to: 302-288-6884 If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe