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Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies

This Disinfection and Cleanroom Cleaning training will teach you how to choose the best disinfectants, know the different performance parameters of disinfectants, methods to qualify disinfectants, writing and executing cleaning procedures.

March 10, 2011 - PRLog -- Selection of best disinfectants, applying right performance parameters and methods to qualify are keys to designing an effective disinfectant validation program to meet FDA, Irish Medical Board, MHRA, and EMEA scrutiny. This webinar provides guidance on industry trends, regulatory feedback, and keys to design for an effective validation program. Current 483's, Warning Letters, and Field Experiences will be conveyed that allow end users to determine that best methods to validate sanitizers, disinfectants, and sporicides against their isolates. Common pitfalls and issues with validation testing and test methods will be discussed in an effort to improve the overall results.

This Disinfection and Cleanroom Cleaning training will teach you how to choose the best and effective disinfectants, know the different performance parameters for qualifying disinfectants, methods to qualify disinfectants, how to translate results to cleaning procedures, how to writing and execute cleaning procedures.

Areas Covered in the Seminar:

- Disinfectants commonly used in the industry, their modes of action, efficacy, and toxicity.
- Understanding the nature of contaminants in the cleanroom and which disinfectants will be effective against them.
- Benefits and drawbacks for using each type of disinfectant used in the Pharmaceutical Industry.
- Bodies that regulate disinfectant manufacturers and testing required by manufacturer’s for label claim.
- Learn disinfectant testing methodologies.
- Review of “real world” examples of disinfectant efficacy tests.
- Troubleshooting problems related to disinfectant efficacy testing.
- Overview of the many methods and variations used for disinfectant qualifications.
- Translation of disinfectant qualification results to cleaning procedures to prevent contamination.
- Cleaning procedures-what should be addressed.
- How to monitor efficacy of the cleaning program.
- Examples of disinfectant validation successes will be discussed.
- FDA observations related to Disinfection and Cleaning.

Who Will Benefit:

This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the Pharmaceutical, Biotech, and Medical Device fields

- QA and QC Managers
- Disinfectant Validation Managers
- Operations Managers
- Cleanroom Managers
- Personnel and contractors that clean and disinfect cleanrooms
- Regulatory Compliance Managers & Environmental Monitoring Managers
- Contract laboratories
- Microbiologists
- Manufacturing personnel
- Validation and facilities personnel
- Cleaning Contractors and in-house cleaning personnel

For more details:

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Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates.

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Location:Palo Alto - California - United States
Industry:Medical, Education
Tags:Compliance Training, Web Event, Web Conferencing, Web Seminar, E-learning, EMEA regulation, Fda Warning Letter, Fda
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