The development of fully automated inspection systems for parenteral products has created
a situation of high expectations regarding productivity and quality improvements. However …

The international drive to achieve higher quality and improved cost effectiveness in
parenteral products has achieved an apparent concensus concerning the utility and …

Numerous companies have ordered fully automated inspections systems as a means of
improving inspection performance and reducing costs. A common complaint made is that …

This article reviews automatic inspection within the pharmaceutical industry and deals, in
particular, with the application of machine vision to these tasks. Although taking some time to …

Abstract Good Manufacturing Practice Regulations, under the Food and Drug Administration
(FDA), stipulate that all pharmaceutical products must be free of any contaminants …

The pharmaceutical industry is characterized by strict quality control measures, with the
need for accurate and efficient defect detection in pharmaceutical tablets to ensure product …

Syringes are arguably the most difficult containers to inspect. Among other obstacles,
syringes require unique handling protocols, and their far-ranging shapes and sizes require …

This chapter provides a description of the motivation for the development and application of
real-time, on-line process monitoring techniques for pharmaceutical lyophilization. A high …

Components of a comprehensive validation program include equipment qualification (EQ),
process engineering and process validation. The EQ portion focuses on the lyophilization …

A visit to a pharmaceutical aseptic processing operation in the 1970s would have some
automation on display, but certainly nothing like what is possible today. Just three decades …