Why your food safety legal register may be missing legislation
Is your food safety legal register incomplete? This article explains how primary, secondary, and consolidated law fit together.
Understanding food legislation in the UK: Why it’s harder than it looks
Understanding food legislation is more complex than it seems; missing links, incorrect scope, & outdated sources lead to non-compliance.
Why do we struggle to close out non conformances?
In this article we discuss the issues around non conformance close out, the causes and what the solution may be.
Why We Need More Than HACCP
HACCP alone won’t cut it anymore. Learn why food, packaging, and distribution businesses need a broader Product Safety Plan — and how Techni-K training makes it practical, not just paperwork.
Combine HACCP and HARPC Plans 10 years on
The importance of combining the HACCP principles with the FDAs HARPC requirements.
Risk assessment
In this article we look at the inputs and outputs of risk assessment and how to make it ‘robust’.
Updating documents due to changes in clause references and terminology
In this article we look at changes to clause references, naming and terminology.
Smart maintenance
Why maintenance is so important, not only to the standard, but also as an essential business control.
What are PFAS and what would legislation to restrict or ban it mean?
You may have heard of PFAS, and that the EU is discussing banning it. In this article, we’ll look at what it is, why it’s an issue and what the publication of legislation may mean to the food industry.
Does your internal audit system truly drive continuous improvement?
Why the number one objective for any business must always be continual improvement of the internal audit programme.
Supplier management of agents and brokers
In this article, we look at what is required by agents and brokers, when supply materials and product to GFSI certified businesses.
Validation and verification explained
What’s HACCP validation and verification.
How to comply with food safety and quality culture
Food safety and quality culture is now a requirement of GFSI recognised schemes, find out what it is and how to comply.
Are supplier assessment questionnaires getting out of control?
Are you getting frustrated by the length and complexity of the supplier questionnaires that you’re being asked to complete?
What’s the difference between food and pharmaceutical products?
In this article we look at the difference between a food product and a pharmaceutical product, and how supplements are certified.
How do you interpret ‘previous audit performance’?
This is how we interpret ‘previous audit performance’ from clause 3.4.1 of BRCGS Food (this applies to the other standards too).
Why root cause analysis shouldn’t be applied to minor non-conformances
This article is written to resolve the confusion around when root cause analysis must be applied to non-conformances.
How a shift in mindset changes how you look at the standards
This time, my ‘light bulb moment’ has been even bigger than normal, so I thought I’d share it with you, as it’s very topical.
CCP – Metal detection
The purpose of the CCP metal detection requires that you understand how your detector works so in this issue we help you learn more about it.
BRCGS certification – How long does it take and what’s the process?
If you’ve decided you want to be a BRCGS certificated site; but aren’t sure where to start, this guide will provide you with everything you need to know.
BRCGS Part III – audit protocol
This article explains the key points of the audit protocol section of the BRCGS standards.
BRC service package – fees
It’s that time of the year again – BRCGS fees go up from 1st August 2022
BRCGS Packaging Issue 7
Everything you need to know about the update BRCGS Packaging Issue 7 – all in one place.
Incidents, emergency situations, withdrawals and recalls
In this article we look at the requirements for incident management, emergency situations, withdrawals and recalls within the food industry.
Managing customer standards
Everything you need to know about calibration
What calibration means, why it’s important, when to do it and how it should be done.
Laboratory controls
Testing methods
Once the risk assessment defines what testing is needed, the next step is to define what testing methods will be used.
Managing the testing and inspection system
The testing and inspection system must be managed following the procedure, which must include a risk assessment, testing methods, corrective and preventive action, trending and review.
Changeover controls
These controls reduce cross contamination and prevent the wrong packaging from being used.
Packing controls
Packing controls ensure that the product goes in the correct printed packaging and that the printing is accurate.
Quantity control
A highly regulated process control, to ensure that the weight, volume and count of the product is accurate.
Material handling
Process controls for material handling, such as debagging, deboxing, rework and recipe control.
Allergen controls
Once the allergen risk assessment has been completed the controls from the assessment must be implemented and effectively managed.
Processing equipment
The equipment that’s used to process the product can have a huge impact on the safety, authenticity, quality and legality of the finished product.
Traceability
Traceability is a critical aspect of process control and therefore fundamental in all certification standards.