Emergency Response

Additional Documentation Request (ADR): How to Respond Inside the Window

7 min read · Last reviewed May 23, 2026

If you received a Medicare Additional Documentation Request (ADR), the response window is set by the contractor type and review posture under the Medicare Program Integrity Manual (CMS Pub. 100-08, Chapter 3). MAC, SMRC, and RAC ADRs use a 45-calendar-day clock; UPIC ADRs use a 30-calendar-day clock. Missing the applicable window auto-denies the claim and damages the practice's posture in any escalated review.

What an ADR actually is and who sent it

An ADR is a written request for medical records and supporting documentation tied to specific Medicare claims. Multiple contractor types issue ADRs and they look similar on first read. Read the letterhead carefully:

Each carries the same first-response procedure but different downstream stakes.

The response clock

The response window depends on which contractor sent the ADR and whether the review is prepayment or postpayment. The Medicare Program Integrity Manual (Chapter 3, § 3.2.3.2) governs response timing. Read the letter to confirm which clock applies:

  • MAC prepayment review — 45 calendar days from the date on the letter.
  • MAC postpayment, SMRC, or RAC review — 45 calendar days from the date on the letter.
  • UPIC prepayment or postpayment review — 30 calendar days.

If documentation is not received within the applicable window, the contractor denies the claim for lack of supporting documentation. The no-response denial authority is 42 CFR § 405.929 and § 405.930, and the appeal procedure begins at 42 CFR § 405.903. The denial flows into the standard five-level appeals process.

Late responses sometimes succeed at the redetermination stage but the burden shifts and the contractor's posture toward the practice has already changed.

First 24 hours

  1. Date-stamp the letter on receipt. Log it in the audit tracker with letter date, contractor, claim count, services involved, and internal owner.
  2. Identify the response deadline as letter date + the applicable window (45 calendar days for MAC, SMRC, or RAC ADRs; 30 calendar days for UPIC ADRs). Calendar it with a 7-day-prior internal deadline so submission is not last-minute.
  3. Pull the claims list. Every ADR identifies specific claims by HICN/MBI, dates of service, claim control numbers, and codes. Reconcile the contractor's list against your billing system.
  4. Issue a litigation hold. No deletion of records, no chart edits, no late-dated documentation. Note any chart entries made after the date of service per practice policy.
  5. Engage the billing manager AND a clinician. Pure billing responses miss the medical-necessity narrative. Pure clinical responses miss the coding and modifier picture.
  6. Decide on counsel. Routine TPE ADRs are usually handled internally with billing-vendor support. UPIC and SMRC ADRs warrant counsel from the start.

What to actually submit

The Medicare Program Integrity Manual (Chapter 3, § 3.2.3.4) describes the records reviewers expect. At minimum, per claim:

  • The signed and dated provider note for the date of service
  • Any orders referenced in the note (labs, imaging, DME, referrals)
  • The results that returned from those orders, where they inform medical necessity
  • The relevant history-and-physical or assessment that establishes the clinical reason for the service
  • Any prior authorization, ABN (Advance Beneficiary Notice), or coverage determination
  • The signed Medicare claim and any superbill or encounter form
  • For DME, the order, the proof of delivery, and the medical-necessity documentation per 42 CFR § 424.57
  • For E/M services, history, exam, and medical decision-making documentation supporting the level billed
  • For procedures, the procedure note, anesthesia record if applicable, and pathology report if applicable
Scenario · Audit response

What would you do?

Your MAC mails an ADR (Additional Documentation Request) on 8 claims billed for 99214 with G0439 (Annual Wellness Visit) on the same day. The letter says response is due in 45 calendar days from the letter date.

Today is day 12. You haven't started the response.

Operational self-diagnosis tool. Not legal advice, not a credential of any kind, not a substitute for counsel. The practice remains responsible for the decision it actually makes.

What NOT to submit, edit, or touch

  • Do not late-date or amend records. Any amendment must follow your records policy and CMS's amendment guidance — dated and signed at the time of the amendment, clearly identified as an addendum, not overwriting the original. A back-dated amendment found on review escalates a routine ADR into a fraud referral.
  • Do not submit irrelevant volume. Reviewers note when a 12-page chart arrives for a 3-page request. It signals disorganization or attempted obfuscation.
  • Do not include marketing material, certifications, or letters of recommendation. They are ignored at best, prejudicial at worst.
  • Do not include the EHR's full audit log unless requested. Audit-log production can become its own discovery exercise.
  • Do not contact the requesting reviewer informally. Communications go through the contact listed on the letter, in writing, and through counsel if engaged.

Submission mechanics

Most MACs accept electronic submission through esMD (Electronic Submission of Medical Documentation) per the CMS esMD program. Paper is permitted but slower and creates chain-of-custody questions. If submitting electronically:

  • Confirm the esMD gateway your billing vendor uses
  • Match each claim to its documents with a coversheet listing claim control number, date of service, and document inventory
  • Capture the submission confirmation and date-stamp it into the audit tracker
  • Retain a duplicate of the exact submission set in the practice's audit folder

For paper submission, send by tracked overnight carrier and retain the tracking confirmation.

What happens after submission

The contractor has standardized review timelines published in the Medicare Program Integrity Manual. Common outcomes:

  • Claim paid — review complete, no further action. Document in the audit tracker.
  • Claim denied with appeal rights — file redetermination within 120 days under 42 CFR § 405.940.
  • Partial denial — pay the supported portion, deny the rest. Same appeal mechanics.
  • TPE Round 2 or 3 notice — failed Round 1; education session offered, then Round 2 begins. See TPE program description.
  • Referral to UPIC or RAC — high-error TPE rounds and patterns suggesting fraud route here.
  • Extrapolated overpayment demand — for postpayment review, contractor may extrapolate sample error rate to the universe of claims under Medicare Program Integrity Manual Chapter 8, § 8.4.

If the response surfaces a coding or documentation issue affecting other paid claims, the 60-day overpayment clock at 42 CFR § 401.305 starts independently. See the Medicare 60-day overpayment rule.

State-law overlay

State Medicaid programs run parallel ADR processes with their own response windows — typically shorter than the federal 45 days. California Medi-Cal records requests through DHCS often run on a 30-day window. Texas HHSC Medicaid records requests are governed by Texas Administrative Code Title 1, Part 15, with response windows tied to the request type. New York OMIG audits follow 18 NYCRR Part 517 timelines. State requests on dual-eligibles can run concurrently with federal ADRs and require parallel response.

When to engage outside healthcare counsel

  • Any UPIC or SMRC ADR
  • TPE Round 3 or any TPE moving to extrapolation
  • Any ADR touching more than 50 claims
  • Any ADR following a whistleblower or employee complaint
  • Any ADR where the practice cannot locate the underlying records
  • Any ADR that surfaces a probable overpayment

How d3rx fits

d3rx maintains the ADR workflow inside the compliance binder: log, response checklist, claim-to-document mapping worksheet, submission record, and post-determination tracker. The binder is a source-grounded administrative aid. It does not represent the practice in any Medicare proceeding, does not provide legal advice, and does not replace counsel. See audit defense for the broader response surface and the compliance binder overview for the program structure.

D3rx compliance guides are administrative documentation aids. They do not certify compliance, provide legal advice, replace counsel, or guarantee an audit outcome. The practice remains responsible for reviewing, adopting, and maintaining its compliance program.

Step 1 · Get the binder

Get the d3rx compliance binder for your practice

Pre-filled to address the gaps this guide coversAdditional Documentation Request (ADR): How to Respond Inside the Window. We will email you the section preview and your binder intake link.

No PHI required. We use your email to send the binder preview and intake link only.

Frequently asked

What happens if I respond on day 46?

The claim denies under the Medicare Program Integrity Manual (CMS Pub. 100-08), Chapter 3, § 3.2.3.8, treated as a non-response. The denial is appealable as a regular Medicare claim denial through the five-level appeals process beginning with redetermination at the MAC. You have 120 days to file the redetermination. Late ADR responses are accepted by some contractors at the redetermination stage; the documentation still has to support medical necessity. Do not skip the response — submit it and appeal.

Can I request an extension on an ADR?

Yes, with caveats. Most MACs grant a one-time extension of up to 14 days if requested before the original deadline with stated cause (records pending from referring provider, staff illness, system outage). UPIC and SMRC ADRs are harder to extend. Request in writing to the contact on the letter and document the response. Do not assume an extension was granted absent written confirmation.

Do I need to submit the entire chart or only what was requested?

Submit exactly what was requested plus any supporting documents that establish medical necessity. The Medicare Program Integrity Manual instructs reviewers to evaluate based on submitted documentation. Submitting too little risks denial for inadequate documentation. Submitting irrelevant volume slows review and signals disorganization. Pull the chart, the orders, the labs and imaging referenced in the orders, the notes that establish the clinical rationale, and any prior authorization or coverage determination.

What if I cannot locate the records?

Submit what exists with a written attestation describing the gap and any reconstruction performed. The MAC will deny for inadequate documentation, but submitting nothing produces both denial AND a contractor finding of non-cooperation that can escalate to UPIC or RAC review. The attestation also becomes important in any subsequent overpayment-rule analysis.

Does responding to an ADR start a 60-day overpayment clock?

An ADR itself does not, but the response process commonly surfaces overpayments. If the chart review demonstrates the billed service was unsupported, the 60-day clock at 42 CFR § 401.305 starts on the date the practice has quantified the overpayment. The MAC's eventual denial is independent of the practice's overpayment-rule obligation.

How many ADRs can a single MAC send?

ADRs are typically issued under prepayment or postpayment review with caps published in the Medicare Program Integrity Manual. Targeted Probe and Educate (TPE) reviews sample 20-40 claims per round across up to three rounds. RAC ADRs are subject to limits published by CMS. UPIC ADRs are not capped and can run broader. The volume itself is a signal: high ADR volume often precedes a UPIC or ZPIC referral.

Turn this into a review-ready binder

The Security Risk Analysis is where this guide becomes documentation you can actually hand to a reviewer — assembled into one review-ready binder. Source-grounded, citation-linked, and explicit about what it does and does not do.

Editorial process. This guide was drafted by an LLM (Anthropic Claude) against primary HHS, OCR, CMS, eCFR, NIST, and state-regulator publications, and edited by the D3rx team for restraint and source fidelity. A named credentialed reviewer (CHC, CHPC, or healthcare attorney) is being engaged to verify citations — see the team page for status. Until that reviewer engagement is finalized, this page does not claim credentialed review.

This article is an administrative documentation aid. It does not certify compliance, provide legal advice, replace counsel, or guarantee an audit outcome. The practice remains responsible for reviewing, adopting, and maintaining its compliance program. References cited link to primary sources at HHS, OCR, CMS, the Code of Federal Regulations, NIST, and state regulators.

Authored by D3rx

D3rx is a healthcare-billing and compliance research aid maintained by D3rx Inc. Articles are drafted by an LLM (Anthropic Claude) against primary HHS, OCR, CMS, eCFR, NIST, and state-regulator publications, and reviewed for restraint and source fidelity by the D3rx team.

Reviewer status: a named credentialed reviewer (CHC, CHPC, or healthcare attorney) is being engaged. Until that engagement is finalized, this page does not claim credentialed review.

Sources & Citations
  1. CMS Pub. 100-08, Chapter 3https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/Downloads/pim83c03.pdf
  2. RAC ADR limitshttps://www.cms.gov/research-statistics-data-and-systems/monitoring-programs/medicare-ffs-compliance-programs/recovery-audit-program
  3. Medicare Program Integrity Manual Chapter 4https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/Downloads/pim83c04.pdf
  4. SMRC Statement of Workhttps://www.cms.gov/research-statistics-data-and-systems/monitoring-programs/medicare-ffs-compliance-programs/medical-review-and-education/smrc
  5. 42 CFR § 405.929https://www.ecfr.gov/current/title-42/part-405/section-405.929
  6. § 405.930https://www.ecfr.gov/current/title-42/part-405/section-405.930
  7. 42 CFR § 405.903https://www.ecfr.gov/current/title-42/part-405/section-405.903
  8. 42 CFR § 424.57https://www.ecfr.gov/current/title-42/chapter-IV/subchapter-B/part-424/subpart-D/section-424.57
  9. CMS esMD programhttps://www.cms.gov/research-statistics-data-and-systems/computer-data-and-systems/esmd
  10. 42 CFR § 405.940https://www.ecfr.gov/current/title-42/chapter-IV/subchapter-B/part-405/subpart-I/section-405.940
  11. TPE program descriptionhttps://www.cms.gov/research-statistics-data-and-systems/monitoring-programs/medicare-ffs-compliance-programs/medical-review-and-education/targeted-probe-and-educate-tpe
  12. Medicare Program Integrity Manual Chapter 8, § 8.4https://www.cms.gov/Regulations-and-Guidance/Guidance/Manuals/Downloads/pim83c08.pdf
  13. 42 CFR § 401.305https://www.ecfr.gov/current/title-42/chapter-IV/subchapter-B/part-401/subpart-D/section-401.305

Sources verified as of May 23, 2026

Research Aid Notice

This guide is a plain-English summary maintained by D3rx for healthcare practice administrators. It is not legal advice, medical advice, or accounting advice. The authoritative source is the cited regulation or agency document. Always confirm with qualified counsel before acting on a specific compliance question affecting your practice.

Related Guides