Maintaining a clean,
disinfected and organized laboratory is crucial to avoiding contamination.
Aseptic technique is one of the most important practices a Microbiologist can
use to minimize contamination.
What is aseptic
technique?
Aseptic technique is a
set of practices used in microbiology when handling microorganisms or other
biological material to prevent sample contamination by microorganisms in the
environment. These practices also provide basic personnel protection from
exposure while handling biological material.
Aspects of aseptic
technique are crucial when performing microbiological testing. Some tests
include, but are not limited to:
1.
Sterility
Testing per USP 71 or ISO 11737
2.
Sterilization
Validation Studies
3.
Disinfection
Validation Studies
4.
Microbial
Enumeration Test per USP 61 and USP 62
5.
Neutralization
Studies
6.
Method
Suitability Test, also known as Bacteriostasis and Fungistasis
7.
Bioburden
Testing
The Canadian Biosafety
Handbook provides guidance on good microbiological practices. The aim is to protect
laboratory personnel and the environment as well as to safeguard the sample
against environmental contaminants. Negative controls are included in
microbiological testing to verify the absence of contamination and demonstrate
that the method does not produce false-positive results.
Here are a few tips to
prevent contamination in the laboratory:
1.
Laboratory
personnel training
2.
Good
Microbiology Practices
3.
Personal
Protective Equipment and Hand Hygiene
4.
A
biosafety program
5.
Use of a
Biological Safety Cabinet for microbiological work
6.
Rigorous
housekeeping, cleaning and disinfection procedures
7.
Continuous
improvement of protocols and practices
Laboratory
contamination can significantly impact the accuracy of results. By adopting good
microbiological practices and best practices in identifying sources of
laboratory contamination as well as implementing corrective and preventative
actions, SteriLabs aims to provide the highest standards of accuracy and
reliability in our results.
My Journey as a Microbiology Intern at SteriLabs: Gaining Hands-On Experience and Industry Insights. Blog post by Grace Woods
September 4, 2024
TAMC, TYMC, and absence test for personal care products, pharmaceuticals, cosmetics, and other products categorized as non-sterile. Blog post by Sneha Mistry
July 1, 2024
FDA’s Guidance on Validation Methods for Reprocessing Medical Devices in Healthcare Settings. Blog post by Dr. Anas Aljabo
March 8, 2024
Choosing the right artificial soil for cleaning validation. Blog post by Andres Dumas
February 18, 2024
Disinfection validation requirements based on the Spaulding classification for medical devices. Blog post by Sneha Mistry
January 3, 2024