Three webinars will cover the over-arching strategy for performing a successful cleaning validation
The data used to determine the success of a cleaning validation is built upon both the effective evaluation of the manufacturing plant and the robustness of the validated analytical method. In order to ensure the safety of the consumer, there must be a high degree of confidence in the analytical results in order to verify the absence of residues at the prescribed limits on the various equipment surfaces. The efficacy of disinfectants must be validated as part of microbiological contamination control.
Reading Scientific Services (RSSL) a specialist in scientific consultancy,is hosting a series of webinars to cover the over-arching strategy for performing a successful cleaning validation, with detail on some of the key factors to consider at both the manufacturing, microbiological and analytical stages, highlighting many common pitfalls to avoid.
The Importance of a Good Plant Inspection to a Successful Cleaning Validation Outcome
Date & Time:18 May 2:00pm - 3:00pm (GMT)
Learning outcomes:
Speaker: Brian Hammond, Cleaning Validation, RSSL Consultant
Key Considerations when Developing Analytical Methods to Support Cleaning Validation
Date & Time: 11 June 2:00pm - 3:00pm (GMT)
Learning outcomes:
Speaker: Steve Alley, Technical Specialist
Validating the Efficacy of Disinfectants
Date & Time: 5 July 2:00pm - 3:00pm (GMT)
Learning Outcomes:
Speaker: Darlington Nwodo, Microbiology Laboratory Manager
