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When the Competition and Markets Authority (CMA) announces a market study, or sends your business an information request, the clock starts immediately, and the quality of your initial response shapes every stage that follows. Understanding how to respond to a CMA market study is essential for general counsel, compliance teams and senior executives who need a structured, defensible workflow rather than ad‑hoc reactions. The Enterprise Act 2002 gives the CMA broad powers to compel the production of documents and data, and the CMA’s early‑2026 guidance signals material changes to the way it expects firms to engage, including the introduction of project roadmaps, clearer information‑request formats and earlier remedies conversations.
This guide sets out the complete CMA market study process, from the moment you learn a study has been launched through document production, privilege handling and post‑production cooperation, updated to reflect the 2026 procedural reforms.
A CMA market study is a formal examination of whether competition in a particular market is working well for consumers. The CMA derives its authority to conduct market studies from Part 4 of the Enterprise Act 2002, supplemented by its own published guidance, Market Studies and Market Investigations: Supplemental Guidance on the CMA’s Approach. A market study differs from a full market investigation: the study is the initial, typically less intrusive phase in which the CMA gathers evidence and consults stakeholders. If the CMA concludes that features of the market prevent, restrict or distort competition, it may make a market investigation reference (MIR), escalating the matter into a more detailed Phase 2 investigation with legally binding remedies powers.
Common triggers include a super‑complaint made by a designated consumer body (to which the CMA must publish a reasoned response within 90 days under section 11 of the Enterprise Act 2002), a referral from a sector regulator, a government request, or the CMA’s own monitoring of markets through complaints data, price analysis or intelligence‑sharing with international competition authorities. The CMA publishes a statement of scope when a study opens, identifying the markets and issues under review and inviting interested parties to submit evidence.
Any firm that operates in the market under review, whether as a supplier, purchaser, intermediary or trade association, may receive a CMA information request. Overseas parent companies with UK subsidiaries are within scope if they supply goods or services in the UK market. From the outset, the response effort should involve in‑house legal counsel (as Response Lead), IT, compliance, finance and at least one senior executive with authority to approve productions and attend CMA meetings.
The CMA can direct information requests at any person or business it considers relevant. This includes direct market participants (suppliers and purchasers), trade associations, professional bodies, customer groups and, critically, non‑UK companies that supply goods or services into the UK market or whose conduct has effects within the UK. If your business has a UK subsidiary, branch or significant customer base, you should assume you may be within scope.
Before a formal request arrives, the Response Lead should confirm that the business has the following readiness elements in place:
Engaging specialist external counsel at this stage, rather than after the request is received, significantly reduces the risk of inadvertent privilege waiver and accelerates every downstream step in the CMA market study process.
The following procedure maps the typical workflow for responding to a CMA information request within a market study. The timeline table below summarises each step, the responsible owner and the typical duration. Individual deadlines vary: the CMA specifies a response date in each information request, and businesses should work backwards from that date to build their internal schedule.
| Step | Who does it (owner) | Typical duration |
|---|---|---|
| Triage and preservation (confirm scope, preserve ESI) | In‑house counsel + IT + Compliance (Response Lead) | 0–48 hours |
| Review information request and map custodians | Response Lead + External competition counsel + IT | 1–7 days |
| Privilege review and prepare privilege log | External counsel (privilege review lead) + legal ops | 3–14 days (ongoing) |
| Collect responsive documents and data export | IT / eDiscovery vendor | 7–30 days (depends on volume) |
| Produce documents to CMA (secure upload) | Response Lead + External counsel | 1–3 days per production tranche |
| Meet CMA / provide witness statements | Senior execs + external counsel | 1–8 weeks (as requested) |
| Post‑production clarifications and remedies discussion | External counsel + senior execs | Weeks 4–16 (or longer if investigation escalates) |
Within the first 48 hours of learning that a market study has been opened, the Response Lead should take the following actions:
Once the information request is in hand, the Response Lead and external counsel should:
Legal professional privilege (LPP) protects confidential communications between a client and their legal adviser made for the purpose of giving or receiving legal advice, as well as documents created for the dominant purpose of litigation. The CMA cannot compel the production of genuinely privileged material, but an improperly asserted claim will attract scrutiny and may be challenged. External counsel should:
Document collection and production is typically the most resource‑intensive phase. Key actions include:
The CMA may request meetings with senior executives, site visits, or written witness statements. These interactions are an opportunity to present the business’s perspective, correct factual inaccuracies and explain the competitive context of the market. External counsel should attend all substantive meetings. Prepare witnesses with a pre‑meeting briefing that covers the scope of the study, key themes and the boundaries of what the CMA is entitled to ask. Written submissions responding to the CMA’s working papers or emerging findings should be factual, evidence‑based and linked to specific documents already produced.
After the initial production, the CMA will often issue follow‑up requests for additional documents, clarifications or supplementary data. Maintain the litigation hold and keep the eDiscovery platform active until the study concludes. Under the 2026 procedural changes, the CMA expects businesses to engage in earlier and more structured remedies discussions. If the CMA signals that it is considering a market investigation reference, the business should prepare a substantive remedies response that proposes practical, proportionate solutions, industry observers expect this proactive posture to carry significant weight in CMA decision‑making.
The documents needed for CMA market studies vary by sector, but the following CMA evidence checklist covers the categories most frequently requested:
| Document | Notes |
|---|---|
| Custodian list and data map | Named custodians, systems, date ranges; provided by IT/Legal (CSV/PDF) |
| Contractual documents (agreements, SOWs, NDAs) | Executed versions and amendments; PDF with native files on request |
| Pricing data and transaction logs | CSV or native database exports with metadata; include timestamps and identifiers |
| Internal communications (email threads, memos) | Export with metadata; privilege‑flagged items logged separately (see template) |
| Market/industry reports and board papers | Board minutes, internal analyses (PDF/Word), indicate author and date |
| Customer and supplier lists, commercial terms | Redact personal data unless specifically required; provide summary tables and sample contracts |
| Marketing materials, advertisements, promotions | Provide copies with dates (PDF, native images) |
| Financial statements and KPIs | Trial balance, P&L by product line if requested |
| Compliance logs and policies | Competition compliance policies, audit logs, training records |
| External lawyer advice (privileged) | Do NOT produce; include privilege log entries with legal basis and brief non‑waiving description |
The CMA’s supplemental guidance expects productions to preserve document metadata (author, date created, date modified, file path, custodian). Bulk email productions should include load files in a standard format. Financial and transactional data should be provided in native format (CSV, Excel) with field descriptions. All deliveries should use the CMA’s secure upload portal or an agreed SFTP channel, unsecured email is not acceptable.
Every document withheld on grounds of legal professional privilege must be recorded in a privilege log. The log should contain sufficient detail for the CMA to assess the claim without waiving the privilege. A recommended structure is set out below:
| Document ID | Custodian | Date | Description (non‑waiving) | Legal basis for privilege | Pages withheld |
|---|---|---|---|---|---|
| DOC‑00142 | J. Smith (General Counsel) | 14 Mar 2025 | Email from General Counsel to CEO re: legal advice on pricing compliance | Legal advice privilege | 3 |
Each entry should identify the type of privilege claimed (legal advice privilege or litigation privilege), the relationship between sender and recipient, and the nature of the communication in broad terms. If only part of a document is privileged, redact the privileged content and produce the remainder, noting the redaction in the log.
Where the CMA requests data that includes third‑party personal data or commercially sensitive information belonging to counterparties, the producing business should apply appropriate redactions and provide a confidentiality ring proposal if necessary. The CMA’s supplemental guidance sets out the process for claiming confidentiality over specific material, including the requirement to provide a non‑confidential version for the public file.
How long does a CMA market study take? There is no single statutory time limit that applies to all market studies, but the CMA’s published guidance indicates that a typical market study lasts approximately 12 months from the publication of the statement of scope to the final report. The CMA publishes a project roadmap at the outset, under the 2026 guidance changes, this roadmap is expected to be more detailed and to include indicative deadlines for each major milestone, including the consultation on provisional findings and the deadline for remedies submissions.
Where the study originates from a super‑complaint, section 11 of the Enterprise Act 2002 requires the CMA to publish its response within 90 days, though the substantive market study may continue beyond that deadline.
Businesses should not rely solely on the CMA’s deadline. A defensible internal schedule should include:
If the CMA’s deadline is shorter than 30 days, which is common for targeted requests, compress the schedule accordingly and escalate resource allocation to the executive committee.
The CMA’s case team will generally consider reasonable, well‑evidenced requests for extensions, provided they are made early and explain the practical reasons for the delay (for example, large data volumes, legacy system access issues or the need to coordinate across multiple jurisdictions). Submit the extension request in writing, proposing a revised timeline and interim deliverables. Waiting until the deadline has passed to seek an extension is one of the most common, and most damaging, pitfalls in the CMA market study process.
The cost of responding to a CMA information request varies significantly depending on the volume of data, the number of custodians, the complexity of privilege issues and whether specialist eDiscovery or forensic IT services are required. There are no filing fees payable to the CMA for responding to a market study. The principal cost categories are set out below.
| Cost category | Billing basis | Notes |
|---|---|---|
| External competition counsel (triage, privilege review, CMA meetings) | Hourly rates | Rates vary by firm seniority and complexity; agree a fee estimate and cap at instruction stage |
| eDiscovery (collection, processing, review platform hosting) | Per GB processed + per reviewer/day | Volume‑dependent; obtain competitive quotes from at least two vendors |
| Forensic IT and data export | Fixed fee per system or per custodian | May include server restoration, legacy system access or mobile device extraction |
| Translation and redaction | Per page | Applicable where non‑English materials are in scope |
| Internal staff time (legal, compliance, finance, executive) | Internal HR cost | Record hours for budgeting and, where applicable, tax deductibility purposes |
| Miscellaneous (secure upload, courier, third‑party expert reports) | Variable | Document in the client billing plan and approval matrix |
Early scoping of the information request, including negotiating proportionate search terms and date ranges with the CMA case team, is the single most effective way to control costs.
In February 2026 the CMA published an update on its approach to market interventions, signalling several changes to the markets toolkit. The key developments include the introduction of more detailed project roadmaps at the start of each study, a proposal to replace the existing two‑phase (market study then market investigation) regime with a single‑phase market review tool, and an expectation that businesses will engage in structured remedies discussions earlier in the process. The CMA also indicated that information requests would be more clearly formatted and that it would publish clearer guidance on the types of evidence it considers most useful.
Businesses should update their response playbooks to reflect the following 2026 changes:
The likely practical effect of the 2026 changes is that businesses will need to conduct privilege reviews more quickly and may face compressed production deadlines. Review your privilege framework now, ensure your eDiscovery vendor can scale at short notice, and consider pre‑populating a privilege log template with standard entries that can be adapted for each request.
| Activity | Legal (Response Lead) | IT | Compliance | Finance | CEO / Board |
|---|---|---|---|---|---|
| Issue litigation hold | Responsible | Accountable | Consulted | Informed | Informed |
| Parse information request | Responsible | Consulted | Consulted | Consulted | Informed |
| Custodian identification | Accountable | Responsible | Consulted | Informed | Informed |
| Privilege review | Responsible | Informed | Informed | Informed | Informed |
| Document production | Accountable | Responsible | Informed | Informed | Informed |
| CMA meetings | Responsible | Informed | Consulted | Consulted | Accountable |
| Remedies engagement | Responsible | Informed | Consulted | Consulted | Accountable |
| Budget approval | Consulted | Informed | Informed | Responsible | Accountable |
Engage specialist external competition counsel immediately if any of the following red flags are present: the information request includes questions about pricing coordination, market sharing or information exchange; the CMA signals that it is considering a market investigation reference; the business has previously been the subject of a CMA or European Commission investigation; or the volume and complexity of responsive data exceeds in‑house capacity. Early escalation is invariably less expensive than remediation after a misstep.
Knowing how to respond to a CMA market study is a practical, operational discipline, not a theoretical exercise. The immediate priorities are issuing a litigation hold, appointing a Response Lead, engaging external counsel and mapping custodians against the CMA’s information request. From there, a structured privilege review, defensible document production and proactive engagement on remedies position the business to manage the study effectively and minimise the risk of escalation. With the 2026 procedural reforms introducing project roadmaps and earlier remedies conversations, businesses that update their response workflows now will be materially better prepared. For tailored guidance, use the Competition, United Kingdom practice area page or search the lawyer directory for UK competition specialists.
This article was produced by Global Law Experts. For specialist advice on this topic, contact Julian Maitland Walker at Maitland Walker LLP, a member of the Global Law Experts network.
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