A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals. It is now possible, as demonstrated by Janssen (1), for drug ...

As recent COVID-19 vaccine facility citations make clear, failure to meet cleaning and sanitization requirements puts patients, facilities, and operators at risk. Keeping pharmaceutical facilities ...

This training is designed for those with responsibility for the design, execution, or validation of cleaning processes which may include operations managers and personnel, validation specialists, ...

Validation engineers design or plan protocols for equipment or processes to produce products meeting internal and external purity, safety, and quality requirements. Natural problem-solvers, ...

The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...

This is a practical based course. We explore the issues and pitfalls you may experience when performing Cleaning Validation. Help, guidance and training is given on techniques to overcome the issues ...