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June 2013 [+] (15 total)
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Meet the Tougher U.S. FDA CGMPs
June 4, 2013
Palo Alto CA US
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Medical Device Reporting for Manufacturers, Importers and Medical Device User Facilities
June 4, 2013
Palo Alto CA US
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Auditing Privacy Companies - Implementing Internal Controls
June 5, 2013
Palo Alto CA US
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Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements
June 5, 2013
Palo Alto CA US
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Interest Rate Risk Management - What the Regulators Want
June 6, 2013
Palo Alto CA US
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Project Management in Human Resources
June 7, 2013
Palo Alto CA US
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Basic Superiority, Non-inferiority, or Equivalence Trials: How, Why and When
June 7, 2013
Palo Alto CA US
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Generic Drug Product Development (ANDA) and Paragraph IV Filing Strategy (Exclusive to the US Market)
June 7, 2013
Palo Alto CA US
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Knowing Your Customer - Monitoring and Auditing for PEPs and Other High Risk Customers
June 11, 2013
Palo Alto CA US
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The 2013 Medical Device Tax - Impact of the New Tax on the Marketing and Sale of Human and Veterinary Medical Devices in the U.S. Today
June 11, 2013
Palo Alto CA US
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Must Have Enterprise Metrics for Financial Operations
June 13, 2013
Palo Alto CA US
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FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance
June 14, 2013
Palo Alto CA US
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Global Medical Device Laws and Regulations: US, EU, and Canada
June 18, 2013
Palo Alto CA US
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Establish Change Control for Pharmaceutical Stability Program
June 18, 2013
Palo Alto CA US
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FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations
June 24, 2013
Palo Alto CA US
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