Overview

Visual inspection continues to be an important element of the manufacturing process and the quality assurance of injectable products. This interactive forum will closely examine the latest developments, preparation and use of inspection standards and practical aspects of manual and automated methods along with the regulatory and compendial requirements that govern them.

PDA will host an exhibition during the forum and the PDA Training and Research Institute (PDA TRI) will offer An Introduction to Visual Inspection immediately following the forum, October 21-22.

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
• Inspection Equipment Suppliers: Applications Development, Machine Design, Sales

Contact

Conference inquiries: 
Jason Brown, Programs Manager
Tel: +1 (301) 656-5900 ext. 131
Email: brown@pda.org