As the packaging industry gears up for SQF, industry members should be well acquainted with the rigors of the program as well as the opportunities it represents. This presentation describes the drivers for SQF in the food packaging industry, the requirements for becoming certified, as well as SQF training options for getting started.
Add logos instead of names; add other food logo (our NOP)
Under contract to FDA, Eastern Research Group, Inc. (ERG) conducted an extensive literature review and an expert elicitation of current food safety problems and the range of preventive controls needed to address them.
training imperative by including it among preventive controls necessary to ensure food safety.FDA is requesting comment on whether it should mandate training for employees and supervisors, including a requirement for records that document trainingWhat kind of produce does the proposed produce safety rule apply to?The proposed rule covers most fruits and vegetables while they are in their raw or natural (unprocessed) state. It would not apply to raw agricultural commodities that are rarely consumed raw, those produced for personal or on-farm consumption, and (with certain documentation) those destined for commercial processing, such as canning, that will adequately reduce microorganisms of public health concern.PS.3 How would the proposed rule define “farm”?The proposed rule would define “farm” to mean a facility in one general physical location devoted to the growing and harvesting of crops, the raising of animals (including seafood) or both. “Farm” includes (i) facilities that pack or hold food, provided that all food used in such activities is grown, raised, or consumed on that farm or another farm under the same ownership; and (ii) facilities that manufacture/process food, provided that all food used in such activities is consumed on that farm or another farm under the same ownership.PS.4 How would the proposed rule define “mixed-type facility” and “farm mixed-type facility?The proposed rule would define “mixed-type facility” to mean an establishment that engages in both activities that are exempt from registration under section 415 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), and activities that require the establishment to be registered. An example of such a facility is a “farm mixed-type facility” which is an establishment that grows and harvests crops or raises animals and may conduct other activities within the farm definition, but also conducts activities that require the establishment to register with FDA under section 415 of the FD&C Act.PS.5 Who would be a “covered farm” under the proposed rule?The proposed rule would define “farm” and “mixed-type facility” (see above). Farms and farm mixed-type facilities that have an average annual monetary value of food sold during the previous 3-year period of more than $25,000 (on a rolling basis) would be “covered farms” under the proposed rule, unless they are eligible for the qualified exemption (see below) and FDA has not withdrawn their qualified exemption.The proposed rule would not apply to farms that have an average annual value of food sold during the previous 3-year period of $25,000 or less. FDA notes, however, that these farms are and will continue to be covered under the adulteration provisions and other applicable provisions of the FD&C Act, whether or not they are included within the scope of this proposed rule.PS.6 What qualified exemption is being proposed for certain farms under the proposed rule? As required by FSMA, certain farms would be exempt from most of the requirements of the proposed rule and would instead be subject to modified requirements. This qualified exemption could be withdrawn under certain circumstances. The following farms would be eligible for the qualified exemption: Farms for which, during the previous 3-year period preceding the applicable calendar year: The average annual monetary value of the food sold directly to qualified end-users during such period exceeded the average annual value of the food sold to all other buyers during that period; ANDThe average annual monetary value of all food sold during such period was less than $500,000, adjusted for inflation.PS.7 How would the proposed rule define “qualified end-user”?The proposed rule would define “qualified end-user” to mean, with respect to a food: The consumer of the food; OR A restaurant or retail food establishment that is located in the same state as the farm that produced the food, or not more than 275 miles from such farm.PS.8 How long will the public have to comment on the proposed rule? The comment period is open for 120 days from the date the proposed rule is published in the Federal Register. See www.regulations.gov.
See binder for all GMP SOPs
Under contract to FDA, Eastern Research Group, Inc. (ERG) conducted an extensive literature review and an expert elicitation of current food safety problems and the range of preventive controls needed to address them.
& now offering Internal Auditing for SQF and GFSI programs
What does it mean? Work instructions shall be available for all employees who carry out tasks that are part of the SQF System, e.g., contribute to meeting regulatory compliance; the food safety, quality and process efficiency controls Identified in the SQF System and customer specifications. What do I have to do? Instructions can be provided in a number of ways such as: •Written work instructions may be useful when a particular task is complicated (i.e., requiring skilledoperators) or repetitious (e.g., mundane work that generally results in a high turnover of staff and requires a constant training effort). These instructions can serve as a valuable training reference when staff needs to check the correct way of doing a task. Written instructions can be in the form of pre-requisite programs (refer 2.3.1 i) and will be available (if practical) where the task is performed. •Photos and diagrams can be particularly useful to overcome language barriers or when a task involves anumber of different steps. Instructions may be included in the food safety andquality manual (2.1.3), and must be kept up to date as process or System requirements change. 2.9.3 Auditing Guidance Work instructions will be assessed at the initial desk audit and compliance at each facility audit byInterview with key personnel, observation of tasks and examination of records. Evidence may include: •There are specific work instructions for maintenance of food safety plan and associated tasks; •There are specific work instructions for maintenance of pre-requisite programs and other tasks relatedGuidance for Developing, Documenting, Implementing,Maintaining and Auditing an SQF System SQF Code, Edition 7.1 – Module 2: SQF System Elements •There are specific work instructions for adherence to customer specifications; •Work instructions are known and applied by personnel conducting food safety and quality tasks; •Work instructions are updated as changes occur to the process or the SQF System.
Almost 85 percent of food companies use on-the-job training, which was closely followed by reading policies, refresher courses and traditional classroom-based learning. It is worth noting that e-learning and interactive training were used by 39 percent and 14 percent of companies, respectively. However, with only 66 percent of companies stating they are very satisfied or satisfied with the quality of training undertaken there is clearly room for improvement. The biggest deficiencies identified were a lack of employee understanding and incomplete training records.