Quality Management Services


Audit Quality Advisory Services for Accounting Firms

Quality Management Services

Quality management is a critical component for firms of all audit practices, including issuer and broker-dealer audits. Firms are required to comply with quality management and quality control standards related to their system of quality management. Specifically, the IAASB, AICPA, and PCAOB have adopted ISQM 1, SQMS 1, and QC 1000, respectively. As a result, firms that are required to follow IAASB, AICPA or PCAOB standards need to reconsider their quality management systems and implement policies and procedures to comply with these requirements.


The following diagrams depicts the steps that a firm should undertake to initially adopt and implement the quality management standards and the iterative and cyclical nature of operating their system of quality management on an annual basis:

Through our experiences evaluating systems of quality control at firms that operate domestically and internationally and completing hundreds of firm inspections, we as Advisors, meet firms where they are and understand the significant effort and the changes required by firms to implement and operate their system of quality management under the new quality management framework. These required changes will affect firms around the globe due to the amount of effort involved given the rigor of these standards. 


We have supported firms' initiatives to establish the appropriate policies, processes and systems to address the changes required in the adoption of the quality management standards. These changes include developing a robust risk assessment process, establishing governance and leadership controls, expanding firm policies and controls around independence and ethics requirements, and identifying and establishing appropriate policies and controls for firm technological, intellectual, and human resources. This work also includes developing or improving processes and controls over monitoring and remediation, including root cause analyses.


JGA has the experience and the team to help firms implement and operate their system of quality management and comply with the quality management standards.

Our Services Include:

Risk Assessment


  • Identify the “what could go wrongs” 
  • Perform a risk evaluation 
  • Assist or perform risk heat mapping development and implementation 
  • Refine and update risks 

Implementation and Training


  • Assist with new or revised control implementation 
  • Support reorganization/realignment 
  • Develop, deliver, and consult on training programs 

Monitoring


  • At firm level 
  • Develop and implement score cards and QC KPIs 
  • At engagement level 
  • Perform pre- and post-inspections 
  • Perform root cause analysis, including
  • interviews with engagement teams 

Evaluation and Testing


  • Assist with the annual evaluation of the system of Quality Management including development, implementation and evaluation 

Quality Management Readiness 


  • Perform an initial risk assessment 
  • Perform a gap health check on key components of the firm’s QC process 
  • Support QC documentation efforts 
  • Advise on software implementation 
  • Refine and assist with developing QC processes 

Root Cause and Remediation 


  • Root Cause 
  • Assist with methodology / audit tool development 
  • Conduct interviews 
  • Perform and analysis of root cause findings 
  • Complete and report on root cause analysis 
  • Remediation 
  • Design and execute on remedial action plans for firm-level deficiencies 
  • Assist with engagement level remediation and resolution
March 30, 2026
In a previous article, Back to Basics: Audit Documentation Failures Have Become Dangerous Low Hanging Fruit , we highlighted how audit documentation had quietly re-emerged as a source of regulatory risk after years of relative deprioritization. While PCAOB Auditing Standard 1215, Audit Documentation (AS 1215), has historically been cited less frequently than other standards, our direct experience from recent inspection activity, enforcement actions, and internal inspection results, demonstrate that documentation failures are increasingly treated as indicators of deeper execution, supervision, and quality management breakdowns. In today’s environment, audit documentation is no longer merely a record of work performed. It is the primary evidence inspectors rely on to evaluate whether an engagement was properly planned, executed, and supported at the time the auditor’s report was issued. What has been low-hanging fruit now requires firms to close these gaps and transform them into a load-bearing foundation for audit quality. From Rare Enforcement to Systemic Inspection Risk AS 1215 establishes clear requirements regarding what must be documented, when documentation must be completed, and how engagement files must be assembled and retained. As discussed in our prior article, failures to comply with these requirements were historically viewed as technical or secondary issues, often resulting in inspection comments rather than enforcement action. That distinction is no longer meaningful. Recent enforcement actions involving backdating, improper (both intentionally, and inadvertent) modification of workpapers, and failure to timely assemble a complete audit file reflect an evolving regulatory view. Documentation failures do not simply violate procedural requirements; they call into question the credibility of the audit opinion itself. More importantly, beyond enforcement, documentation deficiencies are increasingly cited as core inspection findings. Inspectors are challenging situations where engagement teams assert that work was performed but cannot demonstrate that work within the archived file. In these cases, the absence of timely, complete, and clear documentation is no longer treated as a formality. It is treated as evidence that the engagement may not have been properly executed, supervised, or supported in accordance with PCAOB standards. This represents a fundamental shift. Documentation is no longer “low-hanging fruit.” It is a systemic inspection risk that cuts across execution, supervision, and firm-level quality management. From Misconduct to Execution Failures Pervasive documentation failures that do not involve intentional misconduct but still result in non-compliance are increasingly observed. For example, reviewer signoffs occurring near the documentation completion date, rather than contemporaneously with the performance of audit procedures, raise questions about whether effective supervision occurred during the audit or was deferred to meeting archiving deadlines. Similarly, engagement teams may assert that key judgments can be explained verbally, even when those judgments are not clearly documented in the audit file. In today’s environment, the distinction between “we can explain it” and “it is clearly documented” is critical. If procedures, judgments, and conclusions are not evident in the documentation itself, inspectors increasingly conclude that the work was not performed in accordance with PCAOB standards. The issue is not whether the engagement team can explain what they did after the fact. The issue is whether the archived documentation allows an experienced auditor, with no prior connection to the engagement, to understand the procedures performed, evidence obtained, and conclusions reached at the time of the auditor’s report. When documentation fails to reach that standard, inspectors are increasingly concluding that the audit itself was not properly executed, regardless of intent. This reflects an important shift. Documentation failures are no longer viewed primarily as misconduct. They are viewed as symptoms of execution breakdowns, including delayed supervision, compressed review cycles, and audit workflows that defer documentation until the end of the engagement. As a result, AS 1215 has become a direct proxy for how audits are actually performed in practice. How the 14-Day Documentation Completion Requirement Changes the Risk Profile The execution risks are further amplified by the PCAOB’s shortened documentation completion timeline. Recent amendments to AS 1215 reduce the timeframe to assemble a complete and final audit file from 45 days to 14 days after the report release date. While this change may appear procedural, its implications are operational. Under this accelerated timeline, engagement teams no longer have a meaningful post-issuance window to resolve review notes, complete documentation, or finalize supervisory evidence. What were once viewed as “clean-up” activities are now more likely to result in timing violations and non-compliance. This shift places increased emphasis on: Contemporaneous documentation Real-time supervision Realistic workload and staffing models Audit Documentation as a Cornerstone of Audit Quality Audit documentation has long been described as low-hanging fruit in the inspection process. That characterization no longer reflects its role in today’s regulatory environment. Documentation now serves as the primary lens through which regulators assess whether an engagement was properly executed, supervised, and supported. With shortened timelines, expanded quality management expectations, and increased regulatory scrutiny, firms can no longer treat documentation as a downstream activity. It must be embedded into how engagements are planned, staffed, reviewed, and completed. In an environment where inspection conclusions are driven by what is, and what is not, in the audit file, strong documentation is not merely defensive. It is foundational to audit quality. At Johnson Global Advisory , we support firms in selecting, implementing, and optimizing these tools to meet their unique needs. For more insights, visit our blog or contact us to learn how we can help your firm AmplifyQuality®. For more information, please contact your JGA audit quality expert .
January 20, 2026
Introduction The accounting firm industry experienced a ground-breaking transaction in August of 2021 when TowerBrook acquired EisnerAmper, which marked the first private equity (“PE”) transaction of a large-scale accounting firm. This transaction was structured using an alternative practice structure (“APS”). Historically, licensing and independence rules have barred non-CPAs from owning accounting firms. Through an APS, a PE firm may invest in the non-attest entity with service lines such as tax advisory and consulting. The CPA partners retain control over the attest functions, which preserves regulatory compliance. While the APS model has been in existence since the 1990s, this August 2021 transaction brought new attention to this structure. What has followed is an extraordinary volume of deal activity. Per the CPA Trendlines (“CPAT”) Cornerstone report posted on November 18, 2025, CPAT has tracked over 115 PE-related transactions from 2020 to 2025, with over 80 transactions in 2025. While PE in the accounting firm space is no longer news, the pace and volume of transactions is certainly news-worthy. Impact of PE Investment The impact of PE investment on the accounting firm space is unprecedented. The APS has enabled PE to fuel billions of capital investment. PE-backed firms provide immediate payouts to partners at appealing valuations while providing access to capital to these firms for merger and acquisition growth, technology investments, and other priorities. Well-capitalized firms now have an improved ability to invest in technological capabilities, attract experienced talent to be more competitive for college graduates, and improve their market position. With new technologies, routine tasks are being automated such as data entry, tie-outs and controls testing, resulting in less time needed to perform certain audit procedures. What the regulators are saying At the AICPA December 2025 conference on Current SEC and PCAOB Developments, common topics were the presence of private equity in the accounting firm space and the opportunities and challenges that come with this investment. PCAOB Acting PCAOB Chair George Botic described that both transformative technologies (e.g., artificial intelligence or “AI”) and the continuing expansion of private equity investments in accounting firms are two developments that bring opportunities and challenges. Mr. Botic noted that while AI has enhanced risk assessment, reduced manual processes and made it possible to efficiently analyze entire populations of data (which can reduce the risk of missing irregularities or unusual patterns), that overreliance on AI may ultimately threaten auditors’ exercise of professional skepticism and judgment. As it relates to private equity, Mr. Botic noted that while these investments have the potential to enhance audit quality by increasing firm capacity and modernizing audit tools with advanced technologies, the presence of private equity presents a risk that firms shift incentives to prioritize profitability over audit quality. Mr. Botic stated, “Both AI and private equity investments in accounting firms carry the potential to truly reshape the profession. Yet these opportunities come with clear challenges to ensure that overreliance on AI and the pressures of private equity do not jeopardize audit quality.” SEC SEC Chair Atkins discussed in his remarks that he would like the PCAOB to modify its inspections process to place more reliance on the system of quality management and that inspection of certain engagements would inform the PCAOB if the firm’s system of quality management is effective. He also expressed a view that accountability for audit quality should move upward to firm leadership. How is a firm’s system of quality management (“SQM”) impacted? Today’s transforming environment has far-reaching impacts on a firm’s SQM. This publication will focus on risk assessment, governance and leadership, ethics and independence, resources, engagement performance, and monitoring and remediation. 
By Jackson Johnson September 30, 2025
With the effective date for SQMS 1 and QC 1000 fast approaching, firms of all sizes—especially small and sole practitioners—must take action to implement a system of quality management (SQM) that meets the new standards. The good news? You don’t have to start from scratch. Despite QC 1000’s implementation date deferral, the AICPA’s date hasn’t changed, and the international standards are already effective. It’s important to maintain momentum on the efforts toward implementation of all applicable standards for your firm. This article outlines 10 practical steps to help firms build their SQM. Each step includes actionable guidance and considerations for firms with limited resources, and ties into JGA’s broader thought leadership on quality management, risk assessment, and system evaluation. The 10 Steps to Build Your SQM Step 1: Establish a Project Team Form a team with the right mix of quality expertise and operational insight. For small firms, this may mean involving a manager who can grow into a leadership role or setting aside dedicated time as a sole practitioner. Recommended actions to consider: Identify internal champions with interest or experience in quality. Schedule recurring project meetings to maintain momentum. Join a peer group for support and shared learning. Step 2: Understanding and Awareness Document your firm’s business strategy, service offerings, and operational conditions. This step helps identify factors that may impact quality—such as remote work, new industries, or staff turnover. Recommended actions to consider: Conduct a strategy review with firm leadership. List recent changes in firm structure or engagement types. Use these insights to inform your risk assessment. Step 3: Assign Responsibilities Define who is accountable for the SQM. The new standards require clear delineation of ultimate and operational responsibility, including oversight of independence and monitoring. Recommended actions to consider: Assign roles based on existing responsibilities. Clarify delegation boundaries for managing partners. Document responsibilities in your quality manual. Step 4: Establish a Risk Assessment Function Design a process to identify and assess quality risks. This includes understanding conditions or events that could impact quality objectives. Recommended actions to consider: Create a risk assessment policy tailored to your firm. Use relatable examples to demystify risk factors. Leverage AICPA practice aids for structure and templates. Step 5: Perform the Initial Risk Assessment Conduct brainstorming sessions by component and document risks using the AICPA Risk Assessment Template. Include both formal and informal responses. Recommended actions to consider: Use the AICPA risk library to identify common risks. Tailor risks to your firm’s size and services. Include existing responses—even if informal—for evaluation. Step 6: Finalize the Gap Analysis Evaluate where your current responses fall short. This may include undocumented policies or areas where responses don’t fully address the risk. Recommended actions to consider: Identify gaps in governance, ethics, and technology. Determine which informal practices need formalization. Prioritize gaps based on risk severity and regulatory impact. Step 7: Implement Responses to Address the Gaps Develop policies and procedures to close gaps. Responses must be documented and operational. Recommended actions to consider: Draft policies that reflect your firm’s values and risks. Link procedures to specific quality objectives. Use existing documentation as a starting point. Step 8: Update Your Monitoring Process Move beyond peer review prep—monitoring should be continuous and system-wide. Recommended actions to consider: Assign monitoring responsibilities across the team. Incorporate testing of responses into internal inspections. Use dashboards or checklists to track progress. Step 9: Formalize Root Cause and Remediation Procedures Investigate deficiencies and document why they occurred. This step is essential for both system and engagement-level reviews. Recommended actions to consider: Conduct interviews to understand root causes. Use findings to improve policies and training. Apply remediation even if your firm only undergoes engagement reviews. Step 10: Initial Test of Design and Implementation Review documentation and walk through processes to ensure your system is operational and testable. Recommended actions to consider: Validate that each component is supported by evidence. Simulate a peer review to test your system. Confirm that objectives, risks, and responses align. Conclusion Implementing a system of quality management is not just a compliance exercise—it’s an opportunity to strengthen your firm’s foundation for audit quality, risk management, and long-term success. Whether you’re a sole practitioner or a small firm with a few partners, these 10 steps offer a scalable roadmap to meet the new standards. Ready to get started or need help refining your approach? Contact your JGA audit expert today to schedule a consultation and ensure your implementation is tailored to your firm’s needs. At Johnson Global Advisory , we support firms in selecting, implementing, and optimizing these tools to meet their unique needs. For more insights, visit our blog or contact us to learn how we can help your firm AmplifyQuality®.
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July 27, 2026
The Cost of Standing Still Why Inspection Fear Can Create AI Quality Risk In our recent article AI Governance Belongs in the Boardroom, Not the Server Room, we explained why firm leadership must take responsibility for AI governance rather than treating AI as a technology issue. In When AI Becomes a Quality Risk: Why Governance Alone is Not Enough, we examined what happens when governance exists, but validation, monitoring, implementation, and ongoing evaluation fail to keep pace with adoption. This article examines a different risk: what happens when inspection uncertainty causes firms to delay AI adoption? While caution is appropriate, avoiding AI altogether may preserve the very quality challenges firms are trying to solve. The question is no longer simply whether AI can be used safely. The better question is whether the firm can govern AI use intentionally enough to improve audit quality without creating unmanaged risk. Bottom line: Avoidance is not a governance strategy. A firm that refuses to define approved AI use cases may reduce visible adoption, but it may also increase the likelihood of inconsistent practices, informal use, and missed opportunities to address known quality risks. Fear of Inspection Can Become a Quality Management Issue Caution around AI is understandable. Regulators continue to emphasize sufficient appropriate audit evidence, professional skepticism, supervision, documentation, and accountability. AI does not change those expectations, it simply requires firms to demonstrate how AI-assisted work was governed, validated, supervised, and documented. That is why the issue belongs within the system of quality management. AI adoption should not begin with a technology question. It should begin with a quality risk question: where could governed use of AI help the firm respond to recurring quality challenges, and what safeguards must exist before teams rely on the tool? What Inspectors Are Likely to Ask Is Familiar A common misconception is that inspection risk increases simply because a firm uses AI. The more practical risk is that the firm cannot explain how AI use fits within existing audit and quality management expectations. When AI supports audit execution or quality management activities, firms should be prepared to explain: Why the tool was used for a specific audit objective or quality response; How the firm evaluated the reliability, completeness, and relevance of inputs; How outputs were validated before teams relied on them; How professional judgment and skepticism remained central to the conclusion; How firm leadership monitored adoption, consistency, exceptions, and emerging issues. They apply existing expectations to a new way of executing or supporting audit work. A firm that can answer them with clarity is better positioned than a firm that avoids formal AI adoption while informal or inconsistent practices develop outside the quality management framework. Avoidance Can Create Its Own Quality Risks Choosing not to adopt AI may feel like the lower-risk path, particularly for engagements subject to heightened regulatory scrutiny. But avoidance does not eliminate quality risk. In some cases, it preserves deficiencies that technology could help address if implemented with appropriate governance, validation, and monitoring. For example, prolonged hesitation may: Limit the firm’s ability to analyze larger or mor complete populations of data; Maintain manual procedures that are difficult to supervise consistently across engagement teams; Delay improvements to methodology, documentation, training, and review practices; Reduce the firm’s ability to respond to recurring inspection or internal monitoring observations; Create uneven practices where some teams experiment informally while others avoid AI entirely; and Make it harder to attract and retain professionals who expect modern tools and clear guidance. The quality risk is not that every firm must immediately deploy AI broadly. The risk is that leadership may mistake inaction for control. If the firm does not define what is permitted, what is prohibited, and what must be validated, teams may fill the gap themselves. Case Study: When Formal Caution Leads to Informal AI Use Consider a firm that has not approved AI for use in audit execution because leadership is concerned about inspection scrutiny. The firm allows AI for general administrative tasks, but it has not issued detailed guidance addressing engagement-level use, documentation expectations, validation requirements, confidentiality restrictions, or supervision responsibilities. At the engagement level, teams continue to face time pressure, complex documentation requirements, and recurring review notes. Some team members begin using publicly available AI tools to summarize contracts, identify potential risk considerations, draft workpaper language, or explain technical accounting concepts. They do so with good intentions and do not view the use as problematic because the firm has not clearly defined boundaries. Several issues emerge: Governance is unclear because no one has formally approved the use case; Validation practices vary by team member and engagement; Supervision does not fully account for AI involvement; Documentation does not explain how AI-assisted outputs were evaluated; Confidentiality and data protection considerations are inconsistently addressed; and Leadership lacks visibility into how broadly AI is being used in practice. The firm intended to reduce inspection risk by delaying adoption. Instead, it created a more difficult risk profile: informal AI use without a consistent governance structure. From a quality management perspective, the issue is not simply that AI was used. The issue is that the firm did not create a controlled path for responsible use. The Better Question: How Should We Govern Responsible Adoption? Progress begins when firms shift the conversation from whether AI should be used to how AI can be governed as part of the system of quality management. That does not mean approving every tool or every use case. It means creating disciplined pathways for evaluating where AI may support audit quality and where the risks outweigh the benefits. Before expanding AI use, leadership should be able to answer: Which AI use cases are approved, restricted, or prohibited? Which quality risks does each approved use case address? What new risks does the use case introduce? What validation is required before outputs can be used? What documentation should appear in the workpapers or quality management records? Who owns the tool, the methodology, the training, and the monitoring process? How will leadership identify inconsistent uses, exceptions, or emerging concerns? These questions make AI adoption more inspection-ready because they connect the technology to governance, methodology, documentation, supervision, and monitoring. They also help firms avoid the false choice between broad, unmanaged adoption and complete avoidance. Inspection Readiness Comes From Control, Not Inaction Inspection readiness does not require firms to wait for AI-specific regulation. It requires firms to demonstrate that AI use remains grounded in existing audit quality principles: accountability, reliable evidence, professional judgment, supervision, and documentation. A governed approach, including approved uses cases, validation procedures, documentation standards, training, and monitoring, allows firms to innovate while maintaining control. Avoiding AI without addressing informal use often leaves leadership with less evidence of control, not more. Key Takeaways Avoidance is itself a governance decision. Existing audit principles, not new AI rules, remain the foundation for inspection readiness. Informal AI use may create greater inspection risk than transparent, governed adoption. Firms should evaluate AI as a quality response, not only as a technology initiative. Responsible adoption requires approved use cases, validation expectation, accountability, training, documentation standards, and ongoing monitoring. Standing still may preserve known quality challenges while allowing uncontrolled AI practices to develop beneath the surface. Final Thoughts The firms that will be most successful in the AI era are unlikely to be those that adopted AI the fastest or avoided it the longest. They will be the firms that can demonstrate thoughtful governance, disciplined implementation, and continuous oversight. Inspection readiness comes from evidence of control, not evidence of hesitation. Johnson Global Advisory supports firms in developing and evaluating AI governance frameworks, including approved use cases, validation practices, documentation standards, monitoring activities, and accountability structures. An independent review can help leadership assess whether the firm’s approach to AI is disciplined, transparent, and inspection-ready without allowing fear of inspection to slow responsible innovation.
July 16, 2026
In March 2026, the Public Company Accounting Oversight Board (PCAOB) issued a Request for Public Comment as part of its effort to develop a new 2026–2030 strategic plan and reassess future standard-setting priorities. The Board sought stakeholder input on several fundamental questions, including the future direction of inspections and enforcement, the impact of its new quality control standard (QC 1000), enhancements to inspection reporting, standard-setting priorities, international alignment, the role of technology and artificial intelligence, and opportunities to improve transparency with stakeholders. The PCAOB indicated that this feedback would help shape both its strategic plan and future regulatory focus areas.  The response was significant. Stakeholders from across the audit ecosystem—including audit firms, investors, regulators, academics, technology providers, and professional organizations—submitted comment letters addressing how audit oversight should evolve over the next several years. JGA contributed to this dialogue through its own submission to the PCAOB, offering perspectives on inspection modernization, quality management, transparency, and the future of audit oversight. The breadth of feedback provides a valuable view into the challenges, priorities, and expectations shaping the next phase of audit regulation. JGA reviewed 69 comment letters submitted in response to the PCAOB’s request for comment and identified recurring themes across stakeholders. While perspectives vary on implementation, a broader message emerged. Firms are increasingly being asked to demonstrate that audit quality is embedded throughout their organizations, not only within individual engagements. Across stakeholders, there is growing emphasis on system-level quality management, enhanced monitoring, more transparent reporting, stronger emerging technologies, and the ability to respond effectively to evolving regulatory expectations. For many firms, the challenge is no longer simply complying with requirements but demonstrating that audit quality can be sustained at scale. The responses do not call for incremental refinement. They point toward structural change. A System Under Pressure A clear pattern emerged across the comment letters: audit quality is increasingly dependent on access to skilled professionals. For firm leaders, these pressures create practical challenges that extend beyond compliance. Audit firms face increasing difficulty recruiting and retaining experienced professionals while simultaneously responding to expanding regulatory expectations. Many firms must invest in quality control infrastructure, training programs, monitoring activities, and technology enhancements at a time when talent resources are already constrained. This concern is framed not as a near-term challenge, but as a foundational risk to audit quality. The sustainability of the profession, both in terms of talent and institutional capacity, is emerging as a critical issue. At the same time, smaller firms frequently highlighted the disproportionate cost and scalability challenges associated with regulatory compliance, with several respondents warning that increasing complexity may reduce participation among smaller audit providers. Together, these pressures point to a broader tension: how to maintain rigorous oversight while supporting a sustainable and competitive audit market. Reimagining the Inspection Model The most consistent and concentrated feedback across the comment letters relates to the PCAOB’s inspection model. The comment letters suggest that stakeholders increasingly expect inspection programs to provide more context, better severity differentiation, and clearer connections between inspection findings and firm-level quality management systems. Several responses also suggest moving away from binary or pass/fail-style evaluations toward graded or tiered models that better reflect the severity and context of findings. For audit firms, inconsistent inspection outcomes can create uncertainty regarding regulatory expectations, remediation priorities, and resource allocation. When firms are unable to clearly distinguish between systemic quality concerns and less significant documentation deficiencies, it becomes more difficult to prioritize corrective actions and demonstrate the effectiveness of remediation efforts. Taken together, this feedback signals a clear direction- inspection programs must evolve from retrospective, engagement-focused reviews into frameworks that assess how firms operate as systems. Quality Control as the Foundation of Audit Oversight Closely tied to inspection reform is the growing emphasis on quality control systems as the primary driver of audit quality. Perhaps the strongest signal from the comment letters is the growing expectation that audit oversight should focus on the effectiveness of firm’s quality management systems rather than solely on engagement-level outcomes. This includes alignment with emerging frameworks such as QC 1000 and a greater focus on firm-level processes over individual audit outcomes. The implication is significant. Quality is increasingly viewed as systemic, rather than situational, requiring oversight models that evaluate governance, processes, and internal controls at the organizational level. Increasing emphasis on quality control systems requires firms to demonstrate how governance, monitoring, root cause analysis, corrective actions, training, resource management, and accountability mechanisms collectively support audit quality across the organization. From Periodic Review to Continuous Monitoring Another defining theme is the push toward a more data-driven model of audit oversight. Technology providers, data organizations, audit firms, and individual respondents frequently advocated the use of centralized audit data, structured reporting, and analytics-enabled monitoring to support real-time or near real-time oversight. This represents a shift away from periodic, sample-based inspections toward continuous visibility into audit activity. For many firms, this shift raises operational challenges related to data availability, technology infrastructure, governance, and monitoring capabilities. Organizations may need to evaluate whether current systems can support more timely reporting, analytics-enabled monitoring, and greater transparency into quality-related metrics. Technology, in this context, is not viewed as an enhancement, but as an enabler of a fundamentally different oversight model—one built on accessibility, comparability, and timeliness of data. Transparency and Investor Relevance A consistent concern across investors and market participants is the limited usefulness of current reporting outputs. Audit reports, and in particular Critical Audit Matters (CAMs), are frequently described as lacking clarity and specificity. Respondents note that disclosures often fail to provide meaningful insight into what was audited, how risks were addressed, or what the outcomes were. Similarly, PCAOB inspection reports are seen as insufficiently detailed and not clearly connected to investor decision-making. The feedback reflects a broader expectation that audit oversight should produce information that is more transparent, comparable, and meaningful to investors. At a fundamental level, this reflects a broader expectation: that audit oversight should produce outputs that are not only accurate, but usable. AI: A Transformational Force with Governance Implications AI is consistently identified as a transformative force in auditing. Stakeholders recognize its potential to enhance analytics, improve anomaly detection, and increase efficiency. Common recommendations include greater transparency around the use of AI, clear accountability for outcomes, and safeguards to ensure that human judgment remains central to audit conclusions. Interestingly, respondents devoted relatively little attention to AI’s capabilities and significantly more attention to governance, accountability, transparency, and validation. That shift suggests the profession is becoming less concerned with whether AI will be adopted and more concerned with how its use will be governed. The Need for Coordination and Alignment Finally, many respondents highlight the importance of coordination across regulatory and standard-setting bodies. Feedback includes calls for clearer delineation of responsibilities between the PCAOB and other regulators, as well as greater alignment with international standard setters such as the International Auditing and Assurance Standards Board (IAASB). As capital markets continue to operate globally, stakeholders are increasingly focused on consistency across jurisdictions and the reduction of duplication in regulatory requirements. For firms operating across multiple regulatory environments, inconsistent requirements can increase compliance complexity, duplicate effort, and create challenges in maintaining globally consistent methodologies and quality management systems. What makes these themes particularly noteworthy is not that they represent entirely new concerns. Rather, stakeholders from across the audit ecosystem appear to be converging around a common view of where oversight should evolve. The emerging emphasis on quality management systems, transparency, technology-enabled monitoring, and governance suggests that firms may face increasing expectations to demonstrate not only audit execution quality, but also the effectiveness of the systems designed to support it. Converging Signals, Persistent Tensions While the themes across the comment letters are highly consistent, they also reveal important tensions that will shape the next phase of reform: The need for transparency alongside regulatory and legal constraints The balance between innovation and control, particularly in the use of AI The challenge of maintaining investor protection while supporting smaller firms The trade-off between standardized oversight and operational flexibility These tensions are not contradictions. They reflect the complexity of modern audit oversight. What Audit Firms Should Do Now While the future direction of PCAOB oversight will continue to evolve, firms do not need to wait for final regulatory action to prepare. In the near term, audit firms should consider: Evaluating whether their quality control systems are designed, implemented, and documented in a manner that demonstrates firm-level accountability for audit quality. Assessing whether inspection findings, internal monitoring results, and root cause analyses are connected to systemic corrective actions. Reviewing how audit technology, data analytics, and AI-enabled tools are governed, documented, and subject to human oversight. Enhancing transparency in audit committee communications, CAM evaluations, and other reporting outputs. Preparing for oversight models that may place greater emphasis on consistency, scalability, responsiveness, and continuous monitoring. Conclusion While the future direction of PCAOB oversight remains uncertain, the themes emerging from these comment letters point toward a more systemic, transparent, and technology-enabled approach to audit quality oversight. Firms that begin strengthening their quality management systems, monitoring capabilities, governance structures, and reporting practices today may be better positioned to respond to future regulatory expectations and demonstrate sustainable audit quality in an increasingly complex environment. JGA helps audit firms assess, design, and enhance quality control systems, inspection-readiness processes, remediation programs, audit methodology, training, and governance frameworks for emerging technologies. As audit oversight continues to evolve, firms that proactively evaluate their systems, documentation, and monitoring activities will be better positioned to respond to future regulatory expectations.
June 29, 2026
In our recent article, AI Governance Belongs in the Boardroom, Not the Server Room, we explored why firm leadership, not technology teams alone, must take ownership of AI governance. Governance establishes accountability. However, accountability alone does not prevent quality deficiencies. As firms increasingly deploy AI-enabled tools across audit execution and quality management processes, a new challenge is emerging. The very technology intended to improve consistency, efficiency, and audit quality may introduce new risks if governance, validation, and monitoring practices fail to keep pace. For Managing Partners, Chief Quality Officers, and SQMS leaders, the question is no longer whether AI should be adopted. The question is whether the firm’s system of quality management is prepared to govern its use. In this article, we examine a practical question that follows naturally from that discussion: What happens when governance exists, but the firm’s quality management processes fail to keep pace with technology adoption? Governance is Only the Beginning The governance discussion often focuses on who is responsible for AI. Equally important is how firms integrate AI into their systems of quality management. When firms deploy AI-enabled tools to support risk assessment, testing, supervision, or documentation, those tools become part of the firm’s quality response. Technology-related issues rarely present themselves as technology problems. More often, they appear as deficiencies in audit execution, supervision, documentation, or quality management. By the time those deficiencies become visible, the underlying technology considerations may have already affected multiple engagements. As firms evaluate the role of AI within their quality management, one governance question deserves particular attention: Who is accountable when the tool gets it wrong? While technology teams may support implementation, responsibility for how AI-enabled tools influence audit quality resides with firm leadership and the system of quality management. Leadership should evaluate whether AI-enabled tools align with firm methodology, support professional judgement, and introduce risks that require additional oversight. Firms create unnecessary quality risk when they treat AI primarily as an innovation or IT initiative rather than a quality management consideration. How AI Creates Quality Risks The use of AI does not change the auditor’s responsibilities. Requirements relating to audit evidence, professional skepticism, supervision, review, and documentation continue to apply. What changes is the way those risks may manifest. AI can accelerate processes, but it can also accelerate the consequences of weak controls, insufficient oversight, or flawed assumptions. The very technology implemented to improve audit quality may become the source of future inspection findings. AI introduces several audit quality risks, including: Over-reliance on automated outputs Reduced professional skepticism Inconsistent application across engagements Limited transparency around how conclusions are generated Insufficient documentation of judgment Unlike traditional technology risks, these issues may not be immediately visible. Deficiencies often emerge only after engagement teams have relied upon the technology across multiple audits. Firms may use AI-enabled tools to identify unusual journal entries or summarize large data populations. However, when engagement teams rely on AI-generated outputs without sufficiently applying professional judgment, skepticism, and client-specific knowledge, important risk indicators may be overlooked or insufficiently documented. This distinction is important because technology-related issues rarely present themselves as technology problems during an inspection, internal review, or remediation effort. More often, they appear as deficiencies in audit execution, supervision, documentation, or quality management. Through our work supporting firms with inspections, remediation initiatives, and quality management programs, we have observed that the underlying technology considerations are often identified only after broader quality concerns begin to emerge. Case Study: Accelerated Technology and AI Implementation Across our work with firms of varying sizes, we are observing a consistent pattern. Leadership focuses heavily on tool selection and implementation timelines, while significantly less attention is devoted to validation, monitoring, and ongoing evaluation. As a result, firms are discovering quality concerns only after the technology has already been deployed broadly across engagements. Consider a firm that adopted an AI-enabled risk assessment tool as part of its response to inspection findings related to audit execution and documentation. Leadership viewed the implementation as part of its remediation strategy and expected the technology to improve consistency across engagements. However, because validation, methodology updates, training, and monitoring failed to keep pace with implementation, engagement teams began relying on outputs that had not been sufficiently evaluated. Several challenges emerged. The firm had not fully validated the tool’s audit functionality, methodology updates were incomplete, training was limited, and accountability for oversight had not been clearly established. Subsequent post-issuance reviews identified engagement deficiencies directly tied to improper reliance on the tool’s outputs. By that stage, the tool had already been deployed across multiple engagements, amplifying the impact of those deficiencies. The lesson extends beyond implementation. Firms often devote significant effort to deploying new technology but considerably less attention to evaluating outcomes after deployment. Leadership should periodically ask a simple question: Is the tool improving quality? Without ongoing evaluation, firms may assume technology is achieving its intended objectives while quality risks continue to develop beneath the surface. Trusting AI Requires Validation Effective governance requires more than approving technology investments. At its core, validation is about answering a fundamental question: How do we know the output can be trusted? Leaders must understand how the firm validates AI-generated outputs and demonstrates that those outputs support audit objectives. How would the firm demonstrate to an inspector, peer reviewer, or internal reviewer that the tool was appropriately validated and monitored? Before deploying AI-enabled tools, firm leadership should be able to answer: How does this technology support the firm’s audit methodology? What quality risks does it introduce? How will outputs be validated? How will use be monitored across engagements? Final Thoughts Governance establishes accountability, but accountability alone does not ensure audit quality. Firms create risk when they treat AI implementation as a technology project instead of a quality response. The most significant AI risk facing firms today may not be the technology itself. It may be the assumption that implementation alone is sufficient. As firms continue adopting AI-enabled tools, leadership should consider a simple question: If this technology contributes to an engagement deficiency next year, can we demonstrate that we appropriately governed, validated, implemented, and evaluated its use? At Johnson Global Advisory, our perspective is informed by work performed across inspections, remediation efforts, technology risk assessments, and quality management initiatives. As firms continue integrating AI into audit execution and quality management processes, understanding how these areas intersect may become just as important as the technology itself.
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