CLEANING VALIDATION PAPER – PART 2

Methodology for Assessing Product Inactivation During Cleaning Part II: Setting Acceptance Limits of Biopharmaceutical Product Carryover for Equipment Cleaning When multiple products are manufactured using the same equipment, it is important to ensure that potential...

THE FUTURE OF VALVES AND DIAPHRAGMS SUPPLY

THE AUTHOR DISCUSSES ISSUES RELATED TO THE SUPPLY OF SOFT PARTS IN THE BIOPHARMA INDUSTRY. May 1, 2013 By: Steve Jones BioPharm International pp. 32-33  The biopharmaceutical industry has for a long time suffered inconsistent reliability performance of valves and...

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