Packaging and Labeling

Venue: Jersey City

Location: Jersey City, New Jersey, United States

Event Date/Time: Mar 01, 2011 End Date/Time: Mar 02, 2011
Report as Spam


Preliminary Outline:
Global Regulatory Requirements: FDA, European Commission and ICH Guidelines
USP Recommendations for Standardizing Prescription Container Labeling
Regulatory Compliance for Advertising and Promotional Labeling
Extractables and Leachables Testing
CTD and eCTD – Management and Submission of Regulatory Documents for Packaging Materials
Multi-Lingual Product Information and Varying International Requirements - Overcoming the Challenges of Global Label Management
Setting Specifications and Acceptable Quality Levels (AQLs)
Risk Management Optimization
Supplier Qualification, Audits and Supply Agreements
Artwork Generation, Control and Authorization
Examining the Impact of Electronic Labeling
Enhancing Packaging and Labeling through Emerging Technologies and Innovative Methods
Guidance on Container Closure Systems (CCS) for Packaging Human Drugs and Biologics
Plastic Parenteral Vials
Qualification of Pharmaceutical Device Packaging
Latest Developments in Blister Packaging – Materials and Technology
Pharmaceutical Primary Packaging Made from Plastic and Glass
Cold Chain Packaging – Addressing Regulatory Expectations and Distribution Challenges
Utilizing the Latest Anti-Counterfeiting Techniques in Pharmaceutical Labeling
Sustainability – Using Industrial Methods (i.e. Lean Manufacturing, 6-Sigma, FMEA) to reach cost-effective processes and reduce waste