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© 2022 MJH Life Sciences and Pharmaceutical Technology. All rights reserved.
© 2022 MJH Life Sciences™ and Pharmaceutical Technology. All rights reserved.
Equipment and Processing Report
January 20, 2016
Automation and ready-to-fill packaging formats are expected to grow in parenteral fill–finish operations.
The revised USP Chapter Sterile Product Packaging-Integrity Evaluation gives best practices for obtaining reliable data in container closure integrity testing and recommends quantitative deterministic methods rather than probabilistic methods.
Pharma companies reduce the impact of manufacturing on the environment with innovations in energy and waste treatment.