MIPS registry enrollment is an operational project, not a sign-up form. Done well, it leaves your wound care or podiatry practice with a confirmed eligibility status, a registry matched to the patients you actually treat, a working connection to your EHR, and a validated first data feed, plus a plan for the rest of the performance year. Before you start, gather your group’s TINs and each clinician’s NPI, the name and contact details of your EHR administrator, and a draft list of the MIPS measures you hope to report. Rules and thresholds change every year, so confirm anything marked “as of 2026” on qpp.cms.gov before you act on it.

Step 1: Which MIPS Participation Status Applies to Your Practice?

Start with the CMS Quality Payment Program participation status lookup on qpp.cms.gov. Enter each clinician’s NPI individually. Eligibility is determined per NPI and TIN combination, so two clinicians billing under the same TIN can have different results. A newly enrolled clinician, a part-time provider, or a nurse practitioner with lower Medicare volume may be excluded or only eligible to opt in while the rest of the group is required to report.

Next, decide the reporting level:

  • Individual: each clinician reports and is scored on their own NPI/TIN. Each enrolls separately with the registry.
  • Group (TIN-level): the practice reports once and every clinician under the TIN receives the same final score. One enrollment covers the group, but weak performance by one clinician affects everyone.
  • Virtual group: solo practitioners and practices with 10 or fewer clinicians combine for reporting and scoring. This requires a formal written agreement and an election submitted to CMS before the performance year begins (the window has historically run October 1 through December 31 of the prior year), so start early.

Then check the low-volume threshold and opt-in rules for the current performance year on qpp.cms.gov. As of 2026, those criteria are defined by Medicare Part B allowed charges, the number of Part B beneficiaries, and the number of covered professional services: more than $90,000, more than 200 beneficiaries, and more than 200 services. A clinician must exceed all three to be required to report; exceeding one or two may make them eligible to opt in. Because they are revised in rulemaking, do not rely on last year’s numbers. Document the result for every NPI in a simple spreadsheet, since you will reuse it during registry sign-up.

One common mistake is assuming hospital-based wound center clinicians report the way office-based podiatrists do. Clinicians who bill 75% or more of their covered professional services in an inpatient, on-campus outpatient hospital (POS 22), or emergency department setting may qualify for facility-based scoring, which can use the hospital’s Value-Based Purchasing score for the Quality and Cost categories. Many hospital-owned wound centers bill as off-campus outpatient departments (POS 19), which does not count toward that threshold, and CMS uses the higher of the facility-based score or any Quality data you submit. Verify each clinician’s status for the current year before you decide which measures to pay for.

Step 2: Should You Choose a QCDR or a Qualified Registry?

The two options differ in what they can submit. A Qualified Registry submits measures from the CMS-established MIPS measure set. A Qualified Clinical Data Registry (QCDR) can submit those as well, plus its own measures developed for a specialty and approved by CMS for that performance year.

This matters in wound care because many generic measures were built for other specialties. They rarely account for a 60-year-old with a six-month-old wound, diabetes, peripheral arterial disease, and several other comorbidities. A raw healing rate compares that patient to a straightforward case and makes your results look worse than your care deserves. Wound-specific measures with risk adjustment correct for this, so your score reflects the patients you actually treat and holds up when an administrator or payer questions it.

When comparing vendors, use a short checklist:

  • Measure set: are there wound and podiatry measures covering your wound types, including outcome measures?
  • Risk adjustment: is the methodology documented, and which patient variables does it use?
  • CMS approval: is the registry an approved QCDR for the current year, and are the specific measures you want included in that approval?
  • Benchmarks: can you compare your results against peers treating similar patients?
  • Support: who helps you during data mapping, validation, and the submission window?

US Wound & Podiatry Registries operates as a wound-focused QCDR built around these needs. For 2026 it offers eight CMS-approved wound care measures. Confirm its current-year measure list and CMS approval status on the registry’s site and on qpp.cms.gov rather than relying on a prior year’s materials, and apply the same check to any other vendor you shortlist.

Step 3: How Do You Select Measures That Fit Your Patient Population?

The Quality category has generally required six measures, including at least one outcome measure or, if none applies, another high-priority measure. Confirm the current-year requirement and any specialty measure set guidance on qpp.cms.gov, since details can change.

Begin with your case mix, not the measure list. Pull a recent report of your visits by diagnosis and sort them into the groups you actually treat: diabetic foot ulcers, venous leg ulcers, pressure injuries, and hyperbaric patients if you run a program. Then match candidate measures to those groups. A measure about a condition you rarely see will fail on volume however well it is specified.

For each candidate, check three things:

  1. Denominator: estimate how many eligible patients and encounters you will have per clinician or group. Compare that to the measure’s case minimum (generally 20 cases) so it can be scored.
  2. Data completeness: CMS sets a minimum percentage of eligible cases that must be reported for each measure: 75% for 2026, a level CMS has finalized through the 2028 performance year. Verify the current-year figure, and be realistic about whether your documentation can reach it for every patient, not only the straightforward ones.
  3. Data availability: confirm that every element the measure needs is actually recorded in your chart.

Where you have a choice, prefer risk-adjusted outcome measures over process-only measures. Process measures are easier to satisfy, but outcome measures that account for wound duration, size, and comorbidity give administrators and referral partners numbers they can trust. Select a few backup measures as well. If a primary measure falls short on volume during validation, you will want a substitute ready.

Step 4: What Do You Need to Sign Up and Execute the Agreement?

Prepare the enrollment packet before the registry asks for it. You will need:

  • The legal practice name and each TIN
  • The NPI of every clinician who will report
  • A designated primary contact for administration
  • A named quality lead who will own validation and sign-off

Read the registry agreement closely, rather than just signing it. Look at how the registry may use your data, including whether de-identified data is used for benchmarking or research, and how that is disclosed. Confirm a HIPAA business associate agreement is part of the package, since the registry will receive protected health information. Check which clinicians are covered and what happens when someone joins or leaves mid-year.

Ask directly about cost structure. Find out whether fees are per clinician or per group, what the base fee includes, and whether adding measures, extra TINs, or additional support carries extra charges. Get the answers in writing and compare vendors on the same assumptions. Do not budget from assumptions or from another practice’s anecdote.

Finally, confirm deadlines. Ask for the registry’s enrollment deadline for the current performance year and for any internal data cutoff that falls before CMS’s own submission window. Registries often need time to process and verify data, so their cutoff can be earlier than the date you see on qpp.cms.gov. Put both dates on your calendar.

Step 5: How Do You Connect Your EHR Without Double Data Entry?

Clinicians will resist any process that makes them type the same information twice, so settle the data pathway before you finish onboarding. Contact your EHR administrator or vendor and ask whether they support a QCDR integration or a structured data export, and whether the registry has worked with your system before.

There are usually three options:

  • Direct EHR integration: data flows automatically through an interface. This is the lowest burden for clinicians but may require vendor build time or fees.
  • Scheduled structured file extract: the EHR produces a file on a set schedule and your team or the vendor sends it to the registry. This is a common middle path.
  • Registry-based capture in the workflow: clinicians record required elements in a registry tool as part of care. Use this when your EHR cannot export what you need, and keep it brief to avoid duplicate entry.

Next, map the data elements. List what each selected measure requires, such as wound type, location, size, duration, comorbidities, and treatment, and note where each lives in your EHR. The key question is whether it sits in a discrete field or in a free-text note. Discrete fields can be extracted reliably. Narrative text usually cannot.

Free-text wound documentation is the most common source of missing data. If a measure depends on wound duration or diabetes status and the clinician only describes it in a progress note, the registry will see a blank. The fix is to add discrete fields or a structured wound care template for those elements, then train clinicians to use it. Make the change before the test feed in Step 6, so you are not validating data that was never captured.

Step 6: How Do You Validate Your First Data Submission?

Do not wait for year-end to learn whether the feed works. Send a test feed for a small sample of patients, perhaps a few from each clinician and each wound type, and compare what the registry received to the charts. Counts of eligible patients, encounters, and key data elements should match your chart review.

Look for the usual problems:

  • Missing denominators: patients you expected to be eligible do not appear, often because a diagnosis code or encounter type was not mapped.
  • Mismatched NPIs or TINs: a clinician’s data is attributed to the wrong group, or not attributed at all.
  • Date-of-service errors: encounters fall outside the performance period or are shifted by a formatting issue.
  • Blank risk-adjustment variables: comorbidities or wound characteristics that never made it into the feed.

Fix each issue at its source in the EHR mapping or template rather than patching it in the registry, otherwise it will recur with every feed. Once the sample is clean, send a larger extract and review the registry’s preliminary performance rates and data completeness. That review should happen with months left in the performance year, not after the window closes.

Finally, document the validation. Have the quality lead record the date, the sample size, the discrepancies found, the corrections made, and a signed approval. If your data is ever questioned, that record shows the submission was checked and can be defended.

Step 7: What Should You Do After Enrollment to Stay on Track?

Enrollment starts the work rather than finishing it. Set a quarterly review using the registry dashboards, with the quality lead, a clinician representative, and whoever manages the EHR templates. At each review, look at measure performance, data completeness, and case volume per clinician.

The purpose is to find gaps while they can still be closed. If a risk-adjustment variable is routinely blank, fix the template. If one clinician’s volume is too low for a measure to score, consider switching to a backup measure. If completeness is slipping at one site, find out whether staff turnover or a workflow change is the cause.

Also confirm how and when the registry submits to CMS on your behalf. Ask whether you must approve the data first and who receives confirmation. After the submission window closes, check qpp.cms.gov to verify that your final score and performance feedback match what the registry reported, and request a targeted review before the CMS deadline if anything does not match.

Finally, consider what else your outcomes data can do. Structured, risk-adjusted results can support conversations with payers, health system leadership, and coverage decision makers, and registry data has been used in policy advocacy for wound care and hyperbaric services. If you cite a specific example externally, verify it against a named, published source first.

How Do You Confirm the Connection and Schedule Your First Review?

Log in to the registry portal and confirm that every clinician is linked to the correct NPI and TIN and that data is arriving on schedule. Then check qpp.cms.gov to make sure the participation status you documented in Step 1 still matches. Once both agree, put your first quarterly performance review on the calendar and assign the person who will run it.

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