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HomeManufacturing (GMP)Essentials of Disinfectant Efficacy Testing: Ensuring Microbial Control

Essentials of Disinfectant Efficacy Testing: Ensuring Microbial Control

Teachers
Crystal Booth
Category:
Clinical Trials (GCP Training)/ Manufacturing (GMP)/ Medical Device Training/ On-Demand Courses/ Quality/ Regulatory & Compliance/ Research & Development/
Clear
Duration: 90-Minutes
On-Demand
Includes handouts
  • Description
  • Who Should Attend
  • What To Expect

Description

COURSE DESCRIPTION

OVERVIEW

Microbial contamination control is essential in ensuring consumer safety – and consumer confidence. However, contaminants are everywhere, and with constantly-mutating strains of bacteria, keeping your research and manufacturing spaces clean is a daunting and ever-evolving task…especially in controlled environments. A common approach is the use of “disinfectants,” usually described as chemical agents used to reduce the microbial load of controlled environments.  Disinfectants play an important role in controlling microbial contamination on surfaces, but one cannot rely on a single, specific product for all applications, due to bacterial mutation and the different types of contaminants found.

Disinfectant efficacy testing is utilized to measure the effectiveness of chemicals that are used clean, sanitize, or disinfect surfaces. There are many regulations and guidance documents that discuss disinfectant efficacy testing, and establishing a compliant disinfectant efficacy testing package aids in providing clear documentation that the disinfectants employed in a facility have been analyzed as required by these regulations.

This webinar will review the essentials of disinfectant efficacy testing and the industry current thinking of disinfectant rotation.  The session will outline common pitfalls and detail best practices for optimal mitigation of contaminants in your controlled environment.

LEARNING OBJECTIVES

At the completion of this session, you will…

  • Recognize the Essentials of Disinfectant Efficacy Testing
  • Identify which test needs to be used in a specific situation
  • Identify some of the regulations governing the test
  • Avoid common regulatory observations regarding disinfectant efficacy
  • Review some of the various testing methods
  • Review how a method is developed and performed
  • Develop a simple method
  • Establish acceptance criteria
  • Develop an inspection package

Who Should Attend

WHO SHOULD ATTEND

This course will be of benefit to anyone working in a GMP-regulated environment on global or domestic scale, who uses (or manages the use or testing of) disinfectants.   This includes personnel in:

  • Quality
  • Manufacturing
  • Microbiology
  • Other functions that utilize disinfectants

What To Expect

WHAT TO EXPECT

HOW TO PARTICIPATE

This webinar is offered on-demand. With your course purchase, you may view the previously recorded live session at your convenience (available for 30 days). Access to the on-demand webinar will be made available via email within 1 business day after your purchase. To access the course, you need only a computer with internet access and the log-in credentials.

THE TRAINING PLATFORM

Our webinar platform combines the convenience of online training with the live interactivity of the classroom. Quizzes, case studies, break-out sessions, and assessments are often incorporated into the training . Other ancillary materials can be downloaded from the “Handouts & Resources” area in the virtual classroom. Each course purchase includes a completion certificate issued to the participant after the course.

USER AGREEMENT

Your registration fee for a single participant entitles you to one telephone dial-in and one online course log-in per site. Course testing capabilities, stored results for training records, and completion certificates are available for only one registrant per single participant course purchase. For multiple participants, please purchase more than one registration or consider our 5 or 10 participant packages.

Is this course right for me? We’d be happy to help you select the right training course to meet your needs.
Give us a call at 215-675-1800 and use Option 3 (9am – 5pm EST, M-F) for assistance.

About Instructors

Crystal Booth
Pharmaceutical microbiologist with expertise in method validations.

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Clear
Duration: 90-Minutes
On-Demand
Includes handouts

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Upcoming Live Courses

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Cleaning Validation Cleanroom Clinical Trials Cloud CMOs Computer Systems CRAs CROs Data Integrity Device eCTD EMA Equipment Facilities FDA GCP GDP GLP GMP HIPAA Human Error ICH Informed Consent Inspections Instructional Design Management manufacturing Marketing MDR microbial control Process Validation Project Management QMS Quality Quality by Design Quality Risk Management Remote Monitoring Risk Risk-Based Monitoring Root Cause Analysis Site Monitoring SOPs Training Trial Master File Upcoming Courses

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The Life Science Training Institute helps pharma, biotech, and medical device companies build knowledgeable, compliant workforces by providing training from drug discovery through commercialization. We are dedicated to advancing careers of those working to develop new therapies and to protect patient safety.

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