FDA Regulatory Rules for Supply Chain and Manufacturing from 2017 Through 2022

MessageThis Webinar is over
Date May 19, 2017
Time 10:00 AM EDT
Cost $299.00
Short Abstract
In this webinar, we will discuss all essential regulatory rules for Supply Chain and Manufacturing

Key Areas Covered During the Webinar: 

1.Introduction:  Counterfeit Crisis and 2001 Initiative
  • Industry and FDA Response:  Track and Trace
  • Drug Supply Chain Security Act (DSCSA)
  • Continuous auditing systems,  ISO 9000/14000
  • 21CFR Part 11, GMP GLP GCP
2.Governance Regulatory Compliance:  From Board Room to the Frontlines
  • Compliance Management.
  • Proactive Risk Balance.
  • Integrated Risk Management Process.
3 .Compliance
  • Global Standards One (GS-1).
  • Open Serialization Communication Standard and Electronic Product Code Information Services (EPCIS).
  • in close coordination with the FDA and the EMA in Europe; which in turn as set up the standards found in DSCSA.
  • Track and Trace Vendors
  • Product tracing across the value chain
  • Detection response from all to identification of countefet

Registration Information
  • Registration Fee : USD $299
  • For assistance on registration, please send an email tomarketing@biopractice.com or Please call: Ph - 1-646-216-8860


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