Packaging and Labeling Training

Assure compliancebefore an inspection,and prepare your organization for the future of regulation. Within the Packaging and Labeling Quality Management System Training participants will receive a fresh view of new regulations, as well as standardized practices that need to be implemented in order to comply with FDA quality standards. Over the course of the two day training attendees will gain insight on a large scope of packaging and labeling topics including qualifications for personnel, control systems, records and documentation, monitoring devices and FDA expectations. The negative consequences of not being prepared for an FDA inspection can be extremely danger-ous and expensive. This course offers your organization the opportunity to feel secure in your packaging and labeling system, and will reformulate your processes to comply with the standards of a heavily regulated industry.
Register for Upcoming Packaging & Labeling Workshops (Click the date to register):
  • April 25-26, 2012 San Diego, CA
  • October 16-17, 2012 Boston, MA
    		•

    Reasons To Attend:

  • Learn best practices for implementing changes in packaging and labeling operations
  • Interact with instructor and attendees to assure system and regulation under standing
  • Define the components of a packaging and labeling system-based inspection
  • Establish maintenance standards for documentation and reporting
  • Determine validation standards
  • Mitigate risk by addressing compliance before inspection
  • Communicate, train and set qualifications for personnel
  • Assess development and manufacturing practices that will be targeted
  • Provide controls to assure no negative impact on your products quality
  • Understand current legislation and trends set by FDA regulations

    • Meet the Instructor:

    Jim Ingram
    Ingram Consulting Services
    Jim has over 20 years of management experience in the Manufacturing and Packaging of Pharmaceutical, Food and Cosmetic Products (Including over10 years with GlaxoSmithKline). He has had direct responsibility for compliance with government agencies such as FDA, EPA, DEA and DA throughout his career. Processes and training programs developed by Jim have resulted in improved FDA audits and relief from Consent Decrees over the pass 9 years as an independent consultant. Jim received his Associates Degree in Engineering from Central Carolina Technical College and attended Campbell University Business School. He has numerous patents to his credit and is a Certified Packaging Professional with the Institute of Packaging Professionals.

    who should attend

  • Quality Systems Managers
  • QC Specialists
  • Laboratory Managers
  • GMP Compliance Specialists
  • Regulatory Affairs Associates/ Managers
  • Audit Services Managers
  • Quality Engineers
  • Production Managers
  • Manufacturing Supervisors
  • Validation Engineers
  • Compliance Managers
  • Systems Managers
  • Documentation Specialists
    • © Global Strategic Management Institute