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Digitizing Your Food Safety Program

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Many food suppliers are investigating and making early investments in the adoption of digital technology to aid and automate their food safety programs. One area of intense interest has been the increasing application of digital automation within food safety testing programs. As a data and technology leader and practitioner across multiple industries for the past 30 years, I have had the privilege of working with organizations as they seek to build the appropriate plans and business justification for taking on digital transformation initiatives.

The following are the top three questions I am continually asked and the answers that, over time, have provided the information and support needed to help companies through this important transition. Perhaps these are similar to the questions that your leadership is asking you?


David Hatch
Featured Expert: David Hatch, VP Digital Solutions Marketing, Neogen Analytics

What are the actual benefits that digitizing our food safety testing program will yield?

David: During the past six years, I have witnessed the implementation and deployment of approximately 500 digital food safety testing programs across the globe. This is always one of the first questions I am asked, and there is inevitably a challenge in the question… namely – “Our program is solid, we pass our certification and customer audits, so tell me how this will be better than what we are doing today.”

The most tangible benefit, of which there are many, boils down to two metrics of success that I have witnessed consistently, over time and across three decades of work, deliver real, measurable change: Time and Trending.

Time, metrics within food safety scenarios, is characterized as having three components:

  1. “Time-to-information” – reducing the time between an event occurring, and information about that event being communicated to those in need of this knowledge.
  2. “Time-to-decision” – reducing the time from when information is known to the moment when a decision can be made to affect the outcome of whatever the information indicates as needing to be addressed.
  3. “Time-to-Action” – reducing the time from when a decision is made to when the enactment of that decision is carried out.

In the world of food safety, the diagnostic information, policy- and compliance-driven decisions, and the corrective and preventative actions (CAPA) that are mandated by regulation and driven by policy compliance standards, define the effectiveness of a food safety testing program.

Therefore, the ability to decrease these timeframes immediately produces a risk reduction result. When the time between an occurrence of a food safety issue and the completion of a corrective action is reduced, so too is risk reduced. Especially when the issue is deemed to be impacting public safety, brand value, and operational continuity… all of which can yield very costly results if not addressed quickly and accurately.

If information is collected and recorded manually, and is stored in individual paper and spreadsheet files, it is, by definition, made ineffective. The time it takes to manually record the data, or retrieve it when needed, works against the requirement that information be on-tap in real time as issues arise. Digitizing a food safety testing program means, beyond merely putting data into spreadsheets, that information be collected and stored in a data base, whether that is data coming from on-premises testing, or a 3rd-party lab. And that database must be connected to a system that enables immediate access, auto-alerts, and data-driven triggers to enact corrective actions without having to wait for a human to think where to look, or how to combine data from various manual storage files.

Trending is equally important. While speed, as highlighted above, is critical, so too is the continuous collection and analysis of data. The ability to trend your diagnostic results goes further than merely seeing a time series report of testing results. If constructed properly, a trending analysis can provide your team with the ability to become far more preventative than ever before.

Trends allow you to see reoccurrences of issues, and as these grow, an alert engine can offer recommended actions that can prevent the future need for full CAPA scenarios, or worse, response to a regulatory inquiry. As illustrated below, when combined together, Time and Trending can yield significant benefit that, as a result, reduce a significant portion of the risk and costs associated with slow response to manually managed food safety testing data. Further, a digitized system can put your data to work for you, creating a scenario that enables the data itself to find the right person at the right time when thresholds and triggers deem this action to be necessary (see figure below).


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How can we measure Return-on-Investment (ROI) on the cost of moving to a digitally managed program?

David: If the question and answer above are not yet enough to justify the move to a digitally managed testing program, there are three more factors to consider when assessing the return on a digital investment:

Reduction of production downtime: The occurrence and frequency of food safety issues increases the risk of system downtime. If a pathogen detection occurs, a machine, conveyor system or other equipment may need to be temporarily shut down for unplanned cleaning, or in extreme cases, torn down altogether for deep cleaning. Our interactions with over 500 implementations have shown that:

  • Downtime can reach an astounding 500 hours annually, leading to overall costs that some studies put in the range of $20,000 to $30,000 per hour, on average.
  • The financial impact of reducing production downtime by just 90 minutes per week can be dramatic once you’ve added up the week-after-week results. For example, a company operating two facilities with a $30,000/hour downtime cost can gain back $90,000 per week with just 90 minutes regained at each location weekly.

Reduction of Waste/Scrap and Rework: A pathogen positive diagnostic result in a Zone 1 or food contact surface location, or worse yet, within a finished product test, will result in the need to scrap and rework production lots. Each pound of finished product that is scrapped will require rework to make up for lost order fulfillment for customers. It is therefore imperative that when issues are detected, the associated corrective actions quickly and accurately address the situation. In my experience, we show that digital trending and time-to-action improvements can drive business impact – specifically, gaining back just 10% of scrapped food per week can yield significant results. For example:

  • An organization operates two facilities where 500 lbs. of finished product are scrapped each week.
  • The value per pound of finished product, when factoring in all the labor, energy costs and materials, is valued at a conservative cost of $1 per pound.
  • Annually, by reducing time-to-information by just 4 hours per sanitation cycle, the organization was able to realize $400,000 reduction in waste-related costs.

Improve Overall Efficiency: Over the course of several months, we partnered with a large dairy producer to explore how automating a manual EMP process could help drive increased efficiencies, reduce pathogen positives, and ultimately, improve the bottom line (see figure below).


Neogen Test Results Chart


Over time, the analysis gained from automated data gathering enabled new sanitation procedures to implemented, leading to significant efficiency gains:

  • A new baseline of testing volume, test types and correlated sanitation procedures were refined and implemented.
  • A revamped remediation program yielded new corrective action steps that have been proven through the study’s data to be more effective.
  • The FSQA team gained back 25% of their time by eliminating the need for manual reporting, analysis, and spreadsheet-based data preparation.
  • The organization improved corrective action completion time by 50%.

What are the resources and time required for the transition to a digitally automated program?

David: There can be a high degree of ‘fear of change’ involved in any digital transformation initiative. This is not unfounded fear, as horror stories abound regarding large enterprise system implementations and the havoc they can cause. The main consideration in avoiding these outcomes is to ensure the initiative has leadership buy-in and support. This is why the answers to the first two questions above are so important. The path to gaining leadership buy-in is through the ability to connect food safety digitization and automation to tangible business results. If a successful business case can be made utilizing the concepts described above, then the battle for assigning resources and the appropriate implementation timeframes can be achieved.

I started working with food safety teams in 2018, when the existence of food safety testing automation was still at a relatively low adoption rate. In the intervening six years, as adoption has increased, the complexity and timeframes of implementation have decreased significantly. This remains a key area of concern, however, as organizations are struggling to keep up with ongoing staffing shortages and resulting resource constraints. There are two key areas where a digital solution provider must be challenged to prove their ability to support your digital transformation:

  1. Proof of delivery: Due to the relatively recent emergence of digital food safety testing platforms, we have not yet reached a state of maturity where tens of thousands of implementations have defined a standard of known implementation and adoption processes to exist. Therefore, it is critical that you find and work with a provider who will deliver a fully functioning trial of their system, preferably free of charge, for a significant amount of time. This will enable you and your team to experience the full range of capabilities offered, including the onboarding and training program, the length of time it takes, the level of technical acumen your team will be expected to have, and the overall delivery of the benefits described above.
  2. Focus on requirements: Commonly, digital solutions are designed to work within fairly rigid processes and workflows as designed into the system. If you’re lucky, you may find a solution that aligns to your own existing workflows, but all too often, the largest stumbling block is the realization that your new system is not just a digital transformation but also requires a full business process reengineering project in order to conform to the way the software works. Challenge your providers to demonstrate how their solution is flexible enough to enable your team to reduce any process changes to the lowest degree possible. While some new processes will always be inevitable (and potentially helpful!), it should be the hallmark of any provider’s customer support/success team to understand your requirements and configure their solution to enable them without too much drastic change.

To learn more about how digitizing food safety programs can impact business ROI, download our EMP ROI white paper today.

Neogen Analytics

Visit Neogen to learn about digitized food safety

 

 

Frank Yiannas, Walmart

Frank Yiannas Joins iFoodDS Board of Directors

By Food Safety Tech Staff
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Frank Yiannas, Walmart

Frank Yiannas, former Deputy Commissioner for Food Policy and Response at the FDA, has joined the iFoodDS Board of Directors. iFoodDS is a provider of connected traceability, quality and food safety solutions. Yiannas will advise the company on strategy.

During his time at the FDA, Yiannas was responsible for a broad range of priorities, including implementing the Food Traceability Rule under the Food Safety Modernization Act (FSMA). Prior to joining the FDA, he spent more than 30 years in food safety leadership roles with Walmart and the Walt Disney Company.

Yiannas has long been a champion of supply chain innovation and technology, making technology-enabled food traceability in the global supply chain a priority in the FDA’s New Era of Smarter Food Safety initiative.

“Frank is a visionary in the food supply chain, using his insight, knowledge and passion for innovation to enhance food safety and safeguard public health,” said Scott Mathews, CEO of iFoodDS. “We are excited to welcome him to the iFoodDS board of directors. His insights will be invaluable as we pursue our vision of a connected food value chain, enabling better collaboration between trading partners and providing insights on product safety, quality and freshness, ultimately reducing food waste and benefiting food companies and consumers alike.”

“I believe that technology will transform the food supply chain, making it safer for consumers, optimizing it, and creating shared value for all supply chain participants,” said Yiannas. “I’m excited to join the iFoodDS board of directors, and to be part of a company that has the food industry expertise, solution capabilities, and vision to not only help companies comply with FSMA 204 regulation, but to help them ensure continued business success by enabling a safer, more predictable food supply and transparency that protects brands and consumers.”

 

FDA

FDA Expects to Release Blueprint for New Era of Smarter Food Safety Soon

By Food Safety Tech Staff
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FDA

On October 1, Frank Yiannas will be the keynote speaker for the 2020 Food Safety Consortium Virtual Series || The series takes place during the weeks of September 3 through December 17Expect the much-anticipated blueprint for FDA’s New Era of Food Safetyto be released soon. The agency has not provided an exact date but in an update prior to the July 4th holiday, FDA stated it would be rolled it out “in the coming weeks”.

“The challenges we’ve faced during the pandemic have made it clear that the goals we set forth in the New Era blueprint are more important now than ever. Some of them, like enhanced traceability, are particularly meaningful in light of recent events,” Frank Yiannas, FDA’s Deputy Commissioner for Food Policy and Response, stated in an agency consumer update. “What we have learned from the pandemic is that we’re on the right track with the New Era of Smarter Food Safety. The steps that we’ll take will prepare us to protect the safety of our food supply, no matter what challenges we face.”

In addition to the focus on emerging digital technologies, traceability in the supply chain, ensuring safety in the home delivery of food (e-commerce), and food safety culture, FDA will be including the lessons learned from the COVID-19 pandemic as part of the blueprint structure.

FST Soapbox

A Digital Approach to Environmental Monitoring: Let’s Get Proactive!

Technology and automation for safety and surveillance have already impacted nearly every industry in the world. For example, in the United States and many other developed regions, we have just lived through the transformation to electronic health records within the healthcare industry. Prior to that, we lived through the digital transformation of all of our banking information to an online banking platform—now the norm across the world.

However, the food and beverage industry is still learning how technology can improve their organizations. The food safety segment of this market is particularly in need of a digital transformation, as the risk associated with foodborne illness is potentially catastrophic to food companies, and moreso, to the end consumers who are impacted by preventable pathogenic outbreaks.

Along with regulation advancements, such as the timed roll-out of FSMA, the industry continues to work towards a more effective approach to food safety. But most regulations, and advancements in the industry are pointed toward a reactive stance to food safety issues, rather than a preventive stance. For example, although traceability is important in leading investigations to the source and taking remediation steps sooner, a more proactive approach to prevention should be considered when investing in food safety programs.

This is where the importance of an automated environmental monitoring program comes in. To be proactive requires a commitment to embracing data and digital technology. Knowing where to start to effectively pivot your digital approach can be a challenge.

Understanding the following thought process can help you to recognize areas of potential improvement and growth within your environmental monitoring program.

  • Define Your Business Objectives. Ask how profitability and production uptime is connected to food safety issues.
  • Verify Suppliers. Establish protocols for incoming product from external suppliers and validate their food safety performance and ability to maintain a clean facility.
  • Modernize Your Environmental Monitoring Program (EMP). Are you able to confirm that your EMP is being executed consistently? Across all facilities?
  • Understand Data Exhaust. See how your organization’s valuable data can be used to identify trends and accelerate root cause analysis that impact decision-making processes.

Define Your Business Objectives

Food companies large and small are being challenged to implement required processes and procedures to meet the demands of FSMA, and ultimately achieve a more proactive and preventative food safety stance. Transformation in this arena, led by government regulation, and enhanced by standards certification requirements, has highlighted the responsibility of suppliers and manufacturers to protect consumers.

Many organizations are not aware that a single failure in their food safety program could actually be the most devastating profitability risk that the organization faces today. When your organization is focused on production uptime and profitability, it can be easy to overlook the details involved in maintaining a strong food safety program. In reality, though, food safety and profitability are inextricably linked due to the risk of production interruptions that can be caused by safety issues.

Whenever a food recall occurs, it has the potential to start the dominoes falling, with major implications regarding costs, reputational damage, compliance penalties, supply chain interruption, and sales declines. Worse yet, these impacts can last for years after the actual event. By delaying both the importance of recognizing the seriousness of this risk as well as taking necessary steps to prevent it, your organization’s reputation could be on the line.

Unfortunately, planning is often sacrificed when managers fail to implement the proper technological solutions. Fulfilling fundamental documentation requirements involves a smart, automated approach. This is the best way to optimize recall prevention. By incorporating an automated EMP process, a supplier management system, and other FSMA Preventive Controls measures, suppliers ultimately improve the strength of the entire chain for their partners, consumers and themselves.

There are many other facets to food safety, but the EMP is where inspectors and auditors will look to see the indicators of contamination and the efficacy of your sanitation controls. Therefore, it is critical that your organization exhibit not only that you are on top of things and are following your EMP procedures consistently, but that you can analyze and pinpoint issues as they arise, and that you have a track record of corrective actions in response to those issues. This, in-turn, allows you to see where your business objectives are most at-risk.

Regardless of which specific food industry segment your company operates in, or which governing body it reports to, it’s essential to stay informed and compliant with changing regulations in order to reduce the risk of experiencing a recall. In a strategic operational role, intelligent environmental monitoring allows companies to not only proactively work to avoid public health issues, but is vital to retaining a consistent bottom line.

Verify Suppliers

Earlier this year, the FDA heralded what they call a “New Era of Smarter Food Safety”. As technology becomes increasingly accessible, more and more companies are investigating how technology can be used to harness and control the growing complexity of supply chain implications.

The challenge of making sure your organization is doing its due diligence to prevent recalls is further complicated when incorporating outside suppliers. For example, 15% of the United State’s overall food supply is imported from more than 200 other countries, according to the FDA. Making sure the product coming into a facility is also meeting your standards is vital to preventing pathogens from entering your supply chain either through containers, people, or the incoming product itself.

The complexity grows exponentially when we contemplate what this means for tracking food safety across a supply chain of this scope. Generally suppliers are asked to provide verification for the cleanliness of the product they are bringing into your facility. However, by going a step further and establishing test points for the product when it comes in, you will be better equipped to catch pathogens before they can enter into your own supply chain and potentially contaminate other products. While you may already have a good relationship with your suppliers, being able to independently verify the safety of their products and that their own processes are working, creates a mutually beneficial relationship.

Modernize Your Environmental Monitoring Program

Food experts at the World Health Organization headquarters in Geneva discussed the critical nature of ensuring food safety across geographic boundaries, as it is an issue that affects everyone. Incidents of pathogen outbreaks around the world have a direct impact on the health of global citizens, with one in 10 people falling ill due to food contamination.

A traditional EMP allows organizations to continuously verify that their sanitation programs are working by scheduling testing, monitoring results for any signs of pathogens, and maintaining compliance with regulatory bodies. Historically, this type of program is documented in spreadsheets and three-ring binders, but today the acceptance of new tools being offered by vendors and labs are expanding offerings to modernize the monitoring process.

Food safety professionals, many of whom are trained microbiologists, should have better tools at their disposal than spreadsheets that force them to manually sift through data. All regulatory bodies in the food industry have guidelines when it comes to where, what, and when you should be testing in your facilities. Ensuring that this is happening is a basic requirement for meeting regulatory mandates.

By choosing an automated EMP, FSQA teams are able to schedule testing plans including randomization and test point coverage rules, see what testing is being performed when, and obtain all testing data in one system for ease of access before or during an audit. This offers an “always-on” source of audit data and more importantly, trending and root-cause analysis capabilities to find and define actions to remediate recurring problems.

Further, an automated EMP that is integrated with your food safety plan allows you to set up workflows and automatically notify appropriate team members according to your organization’s policies. Each remediation step can be recorded and time stamped as the corrective action moves towards completion.

Understand Data Exhaust

A dominant theme pushed forward by FSMA is the need to document all aspects of your food safety plan, from the written outline to the records indicating proper implementation. Today’s manufacturers face a time of heightened regulation, and with stricter enforcement comes greater requirements for documentation. Automated EMPs not only provide your organization insight into what is happening within your facilities for documentation, it also gives time back to your FSQA team who, instead of spending their days with three ring binders, can analyze and investigate recurring issues in your facility to look for new, innovative ways for the organization to maintain a high standard of quality.

However, effective testing also means reading, understanding and responding to results. It is not enough to simply meet the required volume and frequency of environmental testing metrics. You need to use the resulting information to effect change and improvements by lowering the likeliness of pathogens, allergens and contaminants from entering the food supply chain. The more data collected, the more it leads to true understandings. What testing might show is just the symptoms of the problem—not the root cause of a far bigger problem. As more data is available, it becomes more valuable through the insights that can be gained through trend analysis. This, in turn, moves the conversation to higher levels within the organization who care about ensuring productivity and reducing avoidable risk.

Incorporating your lab into the equation is essential. Find a lab partner that offers an automated testing program that is integrated with their LIMS. Your organization will then be in a better position to ensure results are being responded to in an appropriate time frame.

There are many diagnostic tools in use today, both in-plant and at the lab. Each of these tools generates “data exhaust” in the form of a diagnostic result. But are your data streams being integrated and analyzed to find correlations and potential cause/effect relationships? Or does your ATP device simply record its data to a dedicated laptop or spreadsheet?

Testing, combined with an automated EMP, can allow you to combine data from various diagnostic systems (on-premise or from your lab partner) to identify trends and therefore a more holistic path to remediation. For this to occur, data must be accessible, aggregated and actionable, which an automated EMP achieves.

Forward-thinking companies and facility managers are leveraging valuable software solutions to improve processes, protect reputations, minimize inefficiencies, and simplify multifaceted compliance and audit tasks. Over the next three to five years, numerous organizations will reduce their risk of food recalls by combining their EMPs with analytics capabilities to reduce food risk and improve quality using diagnostic solutions and data assets. This change will be arduous, as all digital transformations in other industries have shown. But, in the end, they have shown the value and long-term success that the food industry now needs to experience.