DEVELOPING THE PREVENTIVE CONTROL PLAN(PCP)

A PCP is a written plan to ensure that food is safe and fit for consumption and conforms to consumer protection requirements.

Preventive control plans are not a new concept for many food businesses. For example, federal meat and fish processors already have in place food safety systems such as the Food Safety Enhancement Program (FSEP).
These programs are examples of a PCP. It is, in fact, an internationally accepted approach based on the Codex Alimentarius General Principles of Food Hygiene. Therefore, the CFIA is allowing companies to use other PCP approaches that have been developed by other food safety authorities, or industry associations.
In brief, A HACCP plan and a PCP are both include a hazard analysis and a description of the control measures applied by a food business operator to ensure food safety.

It is always recommended to ensure that the information in the PCP is tailored for your particular business, foods, and market requirements.

Elements of The Preventive Control Plan

A written PCP includes the following:

1. A hazard analysis that describes the biological, chemical, and physical hazards that are reasonably expected to contaminate the food.
2. Descriptions of the control measures used to control those hazards, and the evidence showing they are effective.
3. Descriptions of the critical control points (CCPs) in your process, including the related: control measures, the critical limits, the monitoring and corrective action procedures.
4. Procedures to verify that the PCP has been implemented as written and is effective at preventing, eliminating or reducing to an acceptable level the hazards in the food.
5. Evidence that you have implemented your written PCP. 6. In addition, the written PCP includes the following:

a) Descriptions of the measures you have in place to meet the consumer protection requirements (such as labelling, packaging, grading, standards of identity and net quantity)
b) The supporting documents such as the information you used to determine your hazards, the rationale for identifying your critical control points, and other data.

Steps of Developing The PCP

Assemble the team

Include key people on your team to cover all aspects of your food operation for developing the PCP. Consider using people that: understand the practical aspects of food operations, such as the process flow, and the technology and equipment used in your facility and are knowledgeable in the area of food safety, including the microbial, chemical and physical hazards related to the food being prepared.

Step 1

Ensure the establishment is operated and maintained as required

The first task is to make sure that the way you operate and maintain the establishment meets the requirements applicable to your operation. The requirements are the basic practices a food business must follow to reduce the risk of introducing hazards to the food through the processing environment.

Step 2

Perform a hazard analysis and establish procedures

The next step is to perform a hazard analysis on your food, determine control measures and document it all by applying the following process.

Step 3

Preventive Control Plan Implementation

Once the PCP developed, you need to implement it into your day-to-day operations. This involves:

1. Staff training.
2. Generating records that show you have implemented your PCP and retaining those records.
3. Verifying that the PCP is implemented as written and is effective in preventing food safety hazards, resulting in compliance with the SFCR.

Maintain the Preventive Control Plan

Once you have developed and implemented your PCP, maintain it by reassessing it at a frequency appropriate to your food business, for example annually, and revising it as necessary. The PCP also needs to be reassessed and revised when:

a) Something is new or has changed. For example, with the regulatory requirements, food produced, ingredients or incoming materials, product formulation, equipment, production flow, processing step or production volumes.
b) A problem has been identified. For example, a deficiency or deviation observed during in-house monitoring or verification procedures, non-compliance identified by CFIA or third-party auditors, customer complaints that reveal a problem with the PCP, food recalls or unsatisfactory laboratory results. Reassessing your plan includes reviewing records and conducting on-site assessments of all preventive controls.

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    For each food product, identify and describe any hazards (biological, chemical and physical) that may be reasonably expected to contaminate the food through: the inputs (ingredients and packaging materials), the processing steps and the traffic flows.

    Identify and describe the control measure(s) that control each hazard in your hazard analysis. Include the following details in the description of your control measures:

    • Description of the tasks involved
    • Details of how the task is carried out
    • The frequency of the task
    • The person responsible for carrying out the task
    • Records: it is a good practice to list any forms you use for the day-to-day collection of information used to record the delivery of tasks and controls.
    • Document the evidence that shows that your control measures are capable of controlling the hazard.

    Determine if there are any critical control points in the process. Critical control points (CCP) are the steps in your process, where a control measure is applied and is essential to prevent or eliminate a hazard or reduce it to an acceptable level.

    Establish verification procedures to demonstrate that the control measures in your PCP are implemented as written and are effective in preventing food safety hazards, resulting in compliance with the SFCR.

    Describe the measures you have in place to meet the applicable consumer protection provisions (such as labelling, packaging, grading, standards of identity and net quantity)

    Which may include:

    • Hazard analysis
    • Written control measures for your food safety hazards, and the evidence that they are effective.
    • CCP documentation, including critical limits, and monitoring, corrective action and verification procedures (and all supporting documents that you used to develop your PCP)
    • Written measures describing how you meet the other requirements such as labelling, packaging, grading, standards of identity and net quantity)