Controlling Clostridium botulinum in low-acid canned foods is the highest-stakes food safety challenge a processor can face. This guide explains the critical factors regulators expect you to validate, from 12D thermal processes and cold spot identification to container integrity and deviation handling, and how to build a defensible, system-level control program that protects consumers and the business.
Validating kill steps for low-moisture foods requires more than equipment setpoints or generic studies. This guide explains CFIA expectations for low-moisture validation, why pathogens like Salmonella are harder to control at low water activity, and how to build a product-specific, defensible kill step program that stands up to audits, recalls, and export scrutiny.
MFHPB-30 and rapid Listeria tests serve very different roles when regulators are involved. This article explains why MFHPB-30 carries the most weight for CFIA decisions on plant closures and reopening, where rapid methods add operational value, and how a hybrid testing strategy reduces downtime while protecting regulatory credibility.
Selecting Listeria testing methods in Canada is now a regulatory and business-critical decision. This guide explains which microbiological methods are acceptable to CFIA and Health Canada, how Category 1, 2, and 3 methods differ, and how to build a Compendium-aligned, defensible testing strategy that protects your data, products, and brand.
Health Canada’s updated Listeria policy has raised expectations for environmental monitoring in ready-to-eat food plants. This guide explains why legacy EMPs fall short, what regulators now expect, and how to redesign a risk-based, data-driven Listeria program that stands up to CFIA and Health Canada scrutiny while supporting stable operations.
When a CFIA inspector arrives without notice, microbiology documentation determines whether the visit stays routine or escalates. This guide explains the microbiology records CFIA expects, common documentation gaps that trigger enforcement, and how to build an audit-ready system that protects your operation, products, and reputation.
Key Takeaways for Executives CFIA looks at your microbiology program as the verification engine of your SFCR Preventive Contro...
Dry foods, such as pistachios, spices, cereals, and milk powders, may appear low risk due to their lack of moisture. But in reality, they can harbor dangerous pathogens like Salmonella, Listeria monocytogenes, and E. coli O157:H7 that can survive for long periods in dry environments (1,2). These organisms don’t need water to persist, and some, like Salmonella, can become more heat-resistant when suspended in low-moisture, high-fat food matrices (3)......
We are pleased to announce that our latest peer-reviewed research article, “Construction and Functional Characterization of a Heterologous Quorum Sensing Circuit in Clostridium sporogenes,” has been officially published in ACS Synthetic Biology....
On Sep 25, 2025, CREM Co Teams, Dr. Zargar, Dr. Rahimifard, and Dr. Lefebre visited the Hans Dairy facility in Mississauga.
Food manufacturers know that a product’s shelf life is critical for quality, safety, and brand reputation. Yet microorganisms – bacteria, yeasts, and molds – can quietly sabotage shelf life, causing spoilage, food safety hazards, and even costly recalls. ...
On August 15, 2025, the Public Health Agency of Canada (PHAC) released an update on the ongoing outbreak of Salmonella ...
On August 15, 2025, the Public Health Agency of Canada (PHAC) released an update on the ongoing outbreak of Salmonella ...
Engineers and biochemists at McMaster University have developed a biogel test that allows untrained users to detect bacterial contamination in ...
A recent study published in Nature Microbiology on June 25. has shed light on a critical aspect of herpesvirus infections. Herpesviruses are a widespread family of viruses ...
Researchers at Nofima developed a faster method to detect Listeria monocytogenes in food products, which is a significant challenge for the ...

















