Abstract
The international drive to achieve higher quality and improved cost effectiveness in parenteral products has achieved an apparent concensus concerning the utility and desirability of automated particulate inspection systems. Any perspective on widespread inspection automation must commence with the establishment of realistic objective standards based on sound scientific principles. Economically acceptable methodology must also be available to achieve validation for new procedures and devices. Standards, techniques, and sampling schemes applicable to evaluation and validation of particulate inspections are discussed.
- Received February 25, 1981.
- Accepted May 12, 1981.
- Copyright © Parenteral Drug Association. All rights reserved.
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