PDA Visual Inspection Forum & TRI Course 2013

Visual inspection continues to be an important element of the manufacturing process and the quality assurance of injectable products. Product inspection provides necessary information for lot release, and, coupled with defect identification, contributes to a strategy of continuous process improvement. Past topics have included selection and qualification of human inspectors, validation of automated inspection systems, recent regulatory activity and country specific inspection requirements.

The 2013 Visual Inspection Forum will provide interactive case studies, explore USP<790> - a new draft chapter in development for visual inspection, and discuss new developments in the field of visual inspection, including contributions to a basic understanding of the sampling and inspection process, practical aspects of manual and automated methods, and the regulatory and compendial requirements that govern.

The meeting will feature an exhibition where attendees can see the latest in commercial inspection hardware and discuss production needs with key suppliers of inspection systems and services.

Learning Objectives
At the completion of this meeting, participants will be able to:
• Identify particulate inspection methods and equipment
• Identify critical parameters that affect the inspection process
•  Develop state-of-the-art methodologies which reflect current industry knowledge
• Describe compendial requirements and regulatory trends to ensure their companies are meeting current and anticipated regulatory expectations
• Implement an effective and economical visual inspection process

Who Should Attend
Pharmaceutical/ Biopharmaceutical Manufacturers
Engineering | Manufacturing | Packaging | Process Development | Quality | Technical Services | Validation Pharmaceutical/Biopharmaceutical Developers
Clinical Supplies | Parenteral Development | Process Development Inspec