Browse Events By Author: eventmanager
Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls. Note : Use these promo…
Dec 17, 2010 12:00 AM - Dec 17, 2010 12:00 AM
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Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This medical device training on Importing and Exporting learn and understand the import and export process for unapproved and approved medical devices and the documentation process involved.…
Dec 16, 2010 12:00 AM - Dec 16, 2010 12:00 AM
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Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : In this Food Recall training learn how to create a crisis response plan, data gathering, investigation phase specifics and how to communicate under different scenarios. Note : Use the…
Dec 07, 2010 12:00 AM - Dec 07, 2010 12:00 AM
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Contact Person : ComplianceOnline; Last Date for the submission of abstract : Not Available ; Description : Understand the steps of a extractables / leachables study, get knowledge about the gap analysis of literature sources and how to design an efficient E/L study.
Aug 04, 2011 12:00 AM - Aug 04, 2011 12:00 AM
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Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This drug development process training Webinar will give an overview of drug development process, the regulatory requirements and the analytical technology used for pharmaceutical analysis …
Jun 08, 2010 12:00 AM - Jun 08, 2010 12:00 AM
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Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : In this training you will learn difference between Out-of-Specification (OOS) and Out-of-trend (OOT), requirements for OOT and how to manage OOT results for FDA compliance.
May 25, 2010 12:00 AM - May 25, 2010 12:00 AM
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Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This Clinical Laboratory Improvement Amendments (CLIA) training will be valuable to CLIA regulated non-waived laboratories that run automated analyzers or semi-quantitative kit tests. Not…
Dec 10, 2010 12:00 AM - Dec 10, 2010 12:00 AM
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Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This import compliance webinar will help you understand the basics of importing and discuss how to create and maintain an import compliance program and implement mandatory internal contro…
Sep 15, 2011 12:00 AM - Sep 15, 2011 12:00 AM
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Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This cGMP training will help you in understanding systematic plan of evaluating cGMP applicable to the IND product cycle, the regulatory mandates (FDA, ICH, CHMP and the EU medicine agenc…
Sep 13, 2011 12:00 AM - Sep 13, 2011 12:00 AM
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Contact Person : ComplianceOnline; Last Date for the submission of abstract : Not Available ; Description : This food contamination control program training will teach you how to develop and document an integrated program to reduce the potential of foreign material contamination and als…
Sep 06, 2011 12:00 AM - Sep 06, 2011 12:00 AM
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Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This ISO 14644-1 training will cover the exact procedure for carrying out particle count testing in pharmaceutical clean rooms. It will focus on statistical analysis of results and report…
Nov 15, 2011 12:00 AM - Nov 15, 2011 12:00 AM
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Contact Person : ComplianceOnline; Last Date for the submission of abstract : Not Available ; Description : This webinar addresses new test methods for quantifying migration of Printing inks on food packaging materials into the packaged food and how they affect food safety law complianc…
Sep 15, 2011 12:00 AM - Sep 15, 2011 12:00 AM
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Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This 90-minute Equipment Qualification training will show how pharmaceutical manufacturers can plan and execute a retrospective/prospective qualification plan for their equipments.
Dec 14, 2011 12:00 AM - Dec 14, 2011 12:00 AM
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Contact Person : Referral; Last Date for the submission of abstract : Not Available ; Description : This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively res…
Dec 01, 2011 12:00 AM - Dec 01, 2011 12:00 AM
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