A robust selection of which product(s) and equipment to validate for cleaning is the cornerstone of a successful cleaning validation program. A strategy for selection of products and equipment for cleaning validation is presented.
Submitted: December 1, 2020
Accepted: February 5, 2021
Cleaning validation requires a significant effort to design a strategic and effective program that is defendable with regulatory agencies. Of primary concern is what to validate. A robust selection of which product(s) and equipment to validate for cleaning is the cornerstone of a successful cleaning validation program. A strategy for selection of products and equipment for cleaning validation is presented.
Richard Forsyth is a Principal Consultant with Forsyth Pharmaceutical Consulting.
Pharmaceutical Technology
Vol. 45, No. 8
August 2021
Pages: 44–51
When referring to this article, please cite it as R. Forsyth, "Grouping Products and Equipment for a Worst-Case Cleaning Validation Study," Pharmaceutical Technology 45 (8) 2021.
about 5 years ago
Putting the Patient at the Heart of Dosage Form Designabout 5 years ago
A Digital Supply Chain Helps Ensure API Qualityabout 5 years ago
Serialization: Reducing Counterfeit Drugs and Increasing Salesabout 5 years ago
Designing Incubators for Cell Therapy Manufacturingabout 5 years ago
Implementing Data Integrity Compliance in a GLP Test Facilityabout 5 years ago
Developing the Best Formulation Partnershipabout 5 years ago
Working Towards Zero Emissionsabout 5 years ago
FDA Prioritizes Vaccine Review and Process Improvementsabout 5 years ago
Drug Pricing Scrutiny Increases in Europe
