What is the primary objective of **SQF**?

**The primary objective of SQF is to provide a rigorous, HACCP-based food safety management system that assures consistent production of safe food products across the supply chain.** Administered by the SQF Institute (SQFI), it integrates **Module 2** (universal system elements like management commitment, HACCP plans, verification, and traceability) with sector-specific Good Practices modules (e.g., **Module 11** for food manufacturing GMPs). This GFSI-benchmarked framework ensures preventive controls, operational PRPs (hygiene, pest control, allergen management), and continuous improvement via the triad: "say what you do," "do what you say," and "prove it" through records.

Who is legally or professionally required to comply with **SQF**?

**SQF compliance is not legally mandated but is a professional requirement for suppliers to major retailers, brand owners, and foodservice providers worldwide.** It applies to organizations in food manufacturing (**Module 2 + Module 11**), storage/distribution, packaging, primary production, pet food, and supplements, based on **Food Sector Categories (FSCs)**. Sites must designate a full-time, on-site **SQF Practitioner** (HACCP-trained, competent in the Code) and implement mandatory **Module 2** elements like food safety policy and approved supplier programs to achieve certification.

Does **SQF** require an external audit or third-party certification?

**Yes, SQF requires external audits by SQFI-licensed Certification Bodies (CBs) accredited to ISO/IEC 17065 for third-party certification.** Initial certification audits cover **Module 2** and applicable GMP modules, followed by annual surveillance and periodic unannounced audits (e.g., every 3 years). Nonconformities are graded (minor=1 pt, major=5 pts, critical=50 pts) with score bands: E (96-100), G (86-95), C (70-85), F (<70). CBs issue 12-month certificates listed in the SQFI directory.

How often should an assessment for **SQF** be performed?

**SQF requires annual external certification audits, with internal audits performed at planned intervals to verify system effectiveness.** **Management review** occurs at least annually (with monthly SQF Practitioner updates), covering audits, CAPAs, complaints, and hazards. Internal audits (mandatory **2.5.5**) must cover all elements, using trained auditors and full-scope checklists. Pre-certification gap assessments are recommended 60-90 days prior, after 30-60 days of records.

What are the consequences of non-compliance with **SQF**?

**Non-compliance with SQF results in graded nonconformities, potential certification denial/suspension, and loss of market access to GFSI-recognized buyers.** Critical nonconformities (e.g., uncontrolled hazards) trigger immediate suspension; majors require evidence within 30 days. Failed audits lead to re-audits, fees, and commercial exclusion from retailers. Systemic issues like weak PRPs or unclosed CAPAs cause recurring scores below 70 (F grade), eroding supplier status.

An **SQF** be mapped to other international frameworks?

**Yes, SQF maps to other GFSI-benchmarked frameworks through shared HACCP principles, management systems, and preventive controls.** Its **Module 2** elements (document control, verification, CAPA, internal audits) align with common structures, enabling layering of **SQF Quality Code** atop existing certifications. GFSI recognition ensures equivalence for FSMA preventive controls and Codex standards, reducing duplicative audits.

What is the first step to begin implementing **SQF**?

**The first step to implement SQF is to register the site in the SQFI assessment database and designate a competent, full-time SQF Practitioner.** Select applicable modules (**Module 2** + sector GMP, e.g., **Module 11**), then conduct a gap assessment against the Code (Edition 9 effective May 2021). Develop the food safety policy signed by senior management, per **2.1.1**.

What is the primary objective of **CIS Controls**?

**The primary objective of CIS Controls is to provide a prioritized set of 18 cybersecurity best practices across 153 safeguards to reduce organizational attack surface and mitigate the most common cyber threats.** CIS Controls v8.1, developed by the Center for Internet Security, focuses on actionable tasks like asset inventory and vulnerability management, organized into Implementation Groups (IG1–IG3) for scalable adoption by organizations of all sizes.

Who is legally or professionally required to comply with **CIS Controls**?

**No organization is universally legally required to comply with CIS Controls, as it is a voluntary, consensus-driven framework rather than a mandated regulation.** Professionally, it applies to all industries and sizes—from SMBs targeting IG1's 56 essential safeguards to enterprises pursuing IG3—especially CISOs, IT managers, and regulated entities using it to demonstrate reasonable security hygiene for insurance, contracts, or state safe harbor provisions like those in Connecticut and Louisiana.

Does **CIS Controls** require an external audit or third-party certification?

**CIS Controls does not require external audits or third-party certification, as it lacks a formal certification program.** Organizations self-assess using tools like CIS Controls Navigator or CIS-CAT against the 153 safeguards and IG1–IG3, with optional validation through internal audits, penetration testing (Control 18), or mappings to certified frameworks for assurance.

How often should an assessment for **CIS Controls** be performed?

**CIS Controls assessments should be performed continuously with automated tools, supplemented by quarterly reviews and annual full reassessments.** Safeguards like Control 1 (asset inventory) and Control 7 (vulnerability management) emphasize ongoing monitoring via active/passive discovery, scans, and metrics tracking to maintain IG1–IG3 maturity amid evolving threats and environments.

What are the consequences of non-compliance with **CIS Controls**?

**Non-compliance with CIS Controls exposes organizations to heightened breach risk, operational disruption, regulatory findings, and litigation, without direct fines since it is voluntary.** Poor hygiene in areas like unpatched assets (Control 7) or weak access (Controls 5–6) enables common attacks, potentially leading to data breaches, recovery costs averaging $4.45M (IBM data), insurance denials, and lost contracts.

An **CIS Controls** be mapped to other international frameworks?

**Yes, CIS Controls v8.1 provides official mappings to frameworks including NIST CSF 2.0, ISO 27001, PCI DSS, and HIPAA.** The CIS Controls Navigator automates crosswalks for over 25 standards, enabling organizations to implement CIS's 153 safeguards as a unified operational layer satisfying multiple compliance regimes efficiently.

What is the first step to begin implementing **CIS Controls**?

**The first step to implement CIS Controls is to secure executive sponsorship and conduct a baseline maturity assessment using CIS RAM or Controls Navigator to determine IG1–IG3 placement.** This identifies gaps in foundational Controls 1–2 (asset/software inventories), enabling a phased roadmap starting with IG1's 56 essential safeguards.

SQF vs CIS Controls

Q: How often should an assessment for **SQF** be performed?

**SQF requires annual external certification audits, with internal audits performed at planned intervals to verify system effectiveness.** **Management review** occurs at least annually (with monthly SQF Practitioner updates), covering audits, CAPAs, complaints, and hazards. Internal audits (mandatory **2.5.5**) must cover all elements, using trained auditors and full-scope checklists. Pre-certification gap assessments are recommended 60-90 days prior, after 30-60 days of records.

Q: What are the consequences of non-compliance with **SQF**?

**Non-compliance with SQF results in graded nonconformities, potential certification denial/suspension, and loss of market access to GFSI-recognized buyers.** Critical nonconformities (e.g., uncontrolled hazards) trigger immediate suspension; majors require evidence within 30 days. Failed audits lead to re-audits, fees, and commercial exclusion from retailers. Systemic issues like weak PRPs or unclosed CAPAs cause recurring scores below 70 (F grade), eroding supplier status.

Q: An **SQF** be mapped to other international frameworks?

**Yes, SQF maps to other GFSI-benchmarked frameworks through shared HACCP principles, management systems, and preventive controls.** Its **Module 2** elements (document control, verification, CAPA, internal audits) align with common structures, enabling layering of **SQF Quality Code** atop existing certifications. GFSI recognition ensures equivalence for FSMA preventive controls and Codex standards, reducing duplicative audits.

Q: What is the first step to begin implementing **SQF**?

**The first step to implement SQF is to register the site in the SQFI assessment database and designate a competent, full-time SQF Practitioner.** Select applicable modules (**Module 2** + sector GMP, e.g., **Module 11**), then conduct a gap assessment against the Code (Edition 9 effective May 2021). Develop the food safety policy signed by senior management, per **2.1.1**.

Q: What is the primary objective of **CIS Controls**?

**The primary objective of CIS Controls is to provide a prioritized set of 18 cybersecurity best practices across 153 safeguards to reduce organizational attack surface and mitigate the most common cyber threats.** CIS Controls v8.1, developed by the Center for Internet Security, focuses on actionable tasks like asset inventory and vulnerability management, organized into Implementation Groups (IG1–IG3) for scalable adoption by organizations of all sizes.

Q: Who is legally or professionally required to comply with **CIS Controls**?

**No organization is universally legally required to comply with CIS Controls, as it is a voluntary, consensus-driven framework rather than a mandated regulation.** Professionally, it applies to all industries and sizes—from SMBs targeting IG1's 56 essential safeguards to enterprises pursuing IG3—especially CISOs, IT managers, and regulated entities using it to demonstrate reasonable security hygiene for insurance, contracts, or state safe harbor provisions like those in Connecticut and Louisiana.

Q: Does **CIS Controls** require an external audit or third-party certification?

**CIS Controls does not require external audits or third-party certification, as it lacks a formal certification program.** Organizations self-assess using tools like CIS Controls Navigator or CIS-CAT against the 153 safeguards and IG1–IG3, with optional validation through internal audits, penetration testing (Control 18), or mappings to certified frameworks for assurance.

Standards Comparison

SQF

Voluntary

2023

GFSI-benchmarked HACCP-based food safety certification standard

CIS Controls

Voluntary

2021

Prioritized cybersecurity framework for cyber hygiene

Quick Verdict

SQF ensures food safety certification for global supply chains via HACCP and GMP audits, while CIS Controls provide prioritized cybersecurity hygiene across all industries. Food companies adopt SQF for market access; all organizations use CIS to reduce breach risks efficiently.

Agile Scaling

SQF

SQF Food Safety Code Edition 9

Cost

€€€

Complexity

High

Implementation Time

6-12 months

Key Features

Modular architecture: universal Module 2 plus sector GMPs
GFSI-benchmarked global food safety certification
Mandatory HACCP-based Food Safety Plan
Full-time onsite SQF Practitioner requirement
Graded audits with unannounced verification

Cybersecurity

CIS Controls

CIS Controls v8.1

Cost

€€€

Complexity

Medium

Implementation Time

12-18 months

Key Features

18 prioritized controls with 153 actionable safeguards
Implementation Groups IG1-IG3 for scalable adoption
Mappings to NIST CSF, ISO 27001, PCI DSS
Free CIS Benchmarks for secure configurations
Asset inventory and vulnerability management focus

Detailed Analysis

A comprehensive look at the specific requirements, scope, and impact of each standard.

SQF Details

What It Is

SQF Food Safety Code Edition 9 is a GFSI-benchmarked certification standard for food safety management across supply chains. It applies HACCP principles with modular structure for sectors like manufacturing and distribution, ensuring consistent preventive controls.

Key Components

**Module 2Universal system elements (management commitment, HACCP plan, verification, traceability).
Sector modules (e.g., Module 11 GMPs for processing).
~200 auditable clauses emphasizing PRPs, food defense, allergens.
Built on Codex HACCP; certification via graded audits.

Why Organizations Use It

Provides market access to retailers, reduces recalls, aligns with FSMA/EU regs. Enhances risk management, supplier controls, resilience. Builds stakeholder trust via credible third-party verification.

Implementation Overview

Phased PDCA: gap analysis, documentation, training, internal audits, certification audit. Suits all sizes/industries globally; requires SQF Practitioner, annual surveillance.

CIS Controls Details

What It Is

CIS Controls v8.1 is a community-driven, prescriptive cybersecurity framework of prioritized best practices to reduce attack surfaces and enhance resilience. It applies across industries and organization sizes, using Implementation Groups (IG1–IG3) for risk-based, scalable adoption.

Key Components

18 Controls with 153 Safeguards, from asset inventory to penetration testing.
Organized into IG1 (56 essential safeguards), IG2, IG3 for maturity progression.
Built on real-world attack data; includes free CIS Benchmarks and mappings to NIST, ISO 27001.
No formal certification; self-assessed compliance via tools like Controls Navigator.

Why Organizations Use It

Mitigates 85% of common attacks, cuts breach costs, speeds compliance.
Meets regulatory references (e.g., HIPAA, PCI DSS); aids insurance, partnerships.
Delivers efficiency, trust; scalable for SMBs to enterprises.

Implementation Overview

**Phased roadmapGovernance, discovery (Controls 1-2), foundational (IG1), expansion (IG2/IG3), validation.
Automation-heavy; 9-18 months typical; all sizes/industries; audits optional.

Key Differences

Aspect	SQF	CIS Controls
Scope	Food safety management, HACCP, GMPs, supply chain	Cybersecurity best practices, asset management, access control
Industry	Food manufacturing, storage, distribution globally	All industries worldwide, technology-agnostic
Nature	Voluntary GFSI-benchmarked certification	Voluntary prioritized cybersecurity framework
Testing	Annual third-party audits, unannounced audits	Self-assessments, maturity model progression
Penalties	Loss of certification, market access denial	No formal penalties, increased breach risk

Scope

SQF

Food safety management, HACCP, GMPs, supply chain

CIS Controls

Cybersecurity best practices, asset management, access control

Industry

SQF

Food manufacturing, storage, distribution globally

CIS Controls

All industries worldwide, technology-agnostic

Nature

SQF

Voluntary GFSI-benchmarked certification

CIS Controls

Voluntary prioritized cybersecurity framework

Testing

SQF

Annual third-party audits, unannounced audits

CIS Controls

Self-assessments, maturity model progression

Penalties

SQF

Loss of certification, market access denial

CIS Controls

No formal penalties, increased breach risk

Frequently Asked Questions

Common questions about SQF and CIS Controls

SQF FAQ

CIS Controls FAQ

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SQF

CIS Controls

Quick Verdict

SQF

Key Features

CIS Controls

Key Features

Detailed Analysis

SQF Details

What It Is

Key Components

Why Organizations Use It

Implementation Overview

CIS Controls Details

What It Is

Key Components

Why Organizations Use It

Implementation Overview

Key Differences

Scope

Industry

Nature

Testing

Penalties

Frequently Asked Questions

SQF FAQ

What is the primary objective of SQF?

Who is legally or professionally required to comply with SQF?

Does SQF require an external audit or third-party certification?

How often should an assessment for SQF be performed?

What are the consequences of non-compliance with SQF?

An SQF be mapped to other international frameworks?

What is the first step to begin implementing SQF?

CIS Controls FAQ

What is the primary objective of CIS Controls?

Who is legally or professionally required to comply with CIS Controls?

Does CIS Controls require an external audit or third-party certification?

How often should an assessment for CIS Controls be performed?

What are the consequences of non-compliance with CIS Controls?

An CIS Controls be mapped to other international frameworks?

What is the first step to begin implementing CIS Controls?

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Thailand PDPA Implementation Guide: Subordinate Regulations for 72-Hour Breach Reporting and Cross-Border Transfers (2022-2024 Rules)

ISO 27701 Implementation Roadmap: Extending Your ISMS to PIMS in 12 Months or Less

Run Maturity Assessments with GRADUM

Check out these other Gradum.io Standards Comparison Pages

COPPA vs APRA CPS 234

CIS Controls vs ISO 28000

PIPL vs ISO/IEC 42001:2023