COURSE ID 2803

Cleaning Validation: Best Practices to Implement an Effective and Compliant Process

AVAILABLE On-demand
90 Minutes

On-Demand

Offering Price
$ 295
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Team Training

When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.

Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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Remember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.

Cleaning Validation is one of the many GMP requirements critical to the production of a drug product or medical device. Unfortunately, product recalls due to inadequate cleaning still occur indicating that implementation of an effective and compliant program is lacking in some companies. Because costly regulatory actions can have a significant negative impact on a company, a better understanding is needed.

This 90-minute accredited ON DENAND training course provides practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable, and informed decision making and activity planning. The course will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, cleaning SOPs, and other appropriate documentation. In addition, participants will understand the requirements for maintaining a validated cleaning process.

This online training will benefit professionals in the Pharmaceutical, Biotechnology, Medical Devices, and other regulated industries.

It will be especially valuable to those working as:

– Quality Engineers

– Validation Engineers

– Managers

– Supervisors

– Operators

– Analysts

– Auditors

– Chemists

– Quality Control

– Manufacturing

– Quality Assurance

– Engineering

– Research & Development

Managers and supervisors of this personnel will also benefit from this training by learning about the challenges faced by them.

course instructor

Joy McElroy
Consultant to the Pharmaceutical and Biotech Industries

Joy McElroy’s Courses
Joy McElroy, has 10 years of experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies. Ms. McElroy specializes in Equipment Qualification, Sterilization, Cleaning Validation, and GMP Compliance Auditing. In 2019 Ms McElroy started her own company, McElroy Training and Consultancy. She currently works with Easi.