2019 - C-TPAT Compliance for FDA-Regulated Industries
Date2019-08-30
Deadline2019-08-30
VenueOnline Event, USA - United States
KeywordsGood Documentation Practices; System Risk Evaluation; IC-TPAT Logistics
Topics/Call fo Papers
C-TPAT program overview and tier strategy
Benefits of joining C-TPAT at a variety of levels
Supply chain management, counterfeit and contraband activities
Security for supply chain management
Standard Operating Procedures (SOPs) and Documentation
Physical and Logical Security
Access, Authentication and Authorization
Risk Assessment, Mitigation and Ongoing Management
Vendor and Partner Management
Training Program
Industry Pitfalls and Best Practices
Benefits of joining C-TPAT at a variety of levels
Supply chain management, counterfeit and contraband activities
Security for supply chain management
Standard Operating Procedures (SOPs) and Documentation
Physical and Logical Security
Access, Authentication and Authorization
Risk Assessment, Mitigation and Ongoing Management
Vendor and Partner Management
Training Program
Industry Pitfalls and Best Practices
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- What to Expect from FDA's Approach to Regulate Medical Software
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- The 2019 4th International Conference on Mechanical, Control and Computer Engineering (ICMCCE2019)
Last modified: 2019-08-15 22:12:41