Public Entity
For public entities, FASB ASC 606 effective date for annual/ interim periods is December 15, 2017.
Fundamental changes in the way contracts must be analyzed and reported may be highly disruptive to laboratories and other healthcare entities
The purpose of the new Financial Accounting Standards Board (FASB) Accounting Standards Codification (ASC) Topic 606 accounting standard is to replace industry-specific accounting methods with a better, more consistent and comparable picture of revenues. It is arguably the biggest change in accounting standards since the Sarbanes-Oxley Act of 2002, will change how companies book revenue, and will affect everything from earnings and taxes to bonuses, commissions and buyout decisions.
It’s expected that the impact on laboratories and diagnostic companies is that cash basis revenue recognition is going to be going away. There is an assumption that in a number of instances, revenue recognition ultimately is going to be accelerated under the new standard.
CASEY HAYES, PARTNER, ERNST & YOUNG LLP
For public entities, FASB ASC 606 effective date for annual/ interim periods is December 15, 2017.
Private calendar year entities have an effective date of December 15, 2018. Early adoption is allowed.
This standard has the potential to affect every entity’s day-to-day accounting and, possibly, the way business is executed through contracts with customers. The standard will eliminate the transaction and industry-specific revenue recognition guidance under current US GAAP and replace it with a principle-based approach for determining revenue recognition.
AMERICAN INSTITUTE OF CPAS (AICPA)
FASB 606 requires companies to determine revenue recognition based on a five-step methodology whose core principle is: Recognize revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.
For healthcare diagnostics providers, it is Step Three–determining the transaction price–that requires further consideration and thought, particularly given the transition to value-based care and the diverse nature of constituents such as hospitals, accountable care networks and post-acute care providers.
Laboratories should expect to review every contract they have with health insurers and Medicare Advantage plans, and to develop a reporting formula for every class or type of contract.
Key Differences Between Legacy GAAP and FASB 606 for Diagnostics Providers
Persuasive evidence vs. Contract
The legacy guideline uses the concept of persuasive evidence–evidence (such as contract or purchase order) of the final understanding between parties about the specific nature and terms of an agreed-upon transaction as a guide.
The new standard dictates (in Step 1) the laboratory will identify contracts with customers–agreements that create legally enforceable rights and obligations–which may be oral, written or implied.The following criteria are required to constitute a contract:
Collectability: Then and Now
Under legacy guidance, collectability being reasonably assured was one of the four revenue recognition criteria. The entire contract price needed to be reasonably assured before revenue could be recognized.
Under the new standard, collectability is not a separate criteria, but is referenced in Step 1, where the customer’s ability and intent to pay is evaluated. Under the new guidance, a company not being paid 100% of its contract price does not negate the contract.
Fixed vs. Variable Consideration
Current guidance dicates that the seller’s price needs to be fixed or determinable. If it isn’t, then revenue cannot be recognized.
Under the new guidance Step 3, Determine the Transaction Price, there is the new concept of nvariable consideration. If an entity is willing to accept a lower price than the stated amount of its contract, whether through discounts, rebates, refunds, credits, price concessions, or implied through past business practices, then this is factored into the varabile consideration estimate that is part of determining the transaction price. Two methods are available for variable consideration:
Expected Value: take the sum of probability weighted amounts within a range to come up with a best estimate. This is the method most likely to apply to diagnostics providers.
Most Likely Amount: use a range using a single amount that is most likely to occur.
Also introduced in Step 3 is the concept of applying a constraint to preventing over-recognition of revenue that would require a future reversal
Special Considerations for Diagnostics Providers
Who Is the Customer?
For diagnostics providers, generally the customer is the patient, and the arrangement can be oral or evidenced through established business practices. But the contract must have commercial substance for the revenue to be recognized, and both parties must have the intent and ability to uphold their respective obligations.
Does the Contract Exist?
Diagnostics providers need to look at patient enrollment forms or other documents signed by the patient to determine whether a contract exists. This may require an analysis of specific circumstances to assess enforceability. Also important is collectability criteria:
If there is no history and no evidence of consideration collected, then this would indicate no presence of contract, and therefore the revenue would not be recognizable until a contract exists.
In evaluating collectability, laboratories don’t need to look at individual contract or test or accession, but can group payors into portfolio groups and use that as basis for concluding they’ve met the collectability criteria.
Implicit Price Concessions?
Laboratories need to consider all information that is reasonably available, including historical, current, and forecasted, to estimate the true transaction price for a patient and/or payor. Even if a price concession is only implied, it constitutes a reduction in revenue and needs to be captured that way.
Whereas in the past, such concessions were reflected in bad debt, under new guidance they are taken as a revenue reduction. Bad debt is reserved for impairments such as bankruptcy or change in credit, not “true-ups” to variable consideration.
Developing an Estimate
Use of historical experience to estimate adjustments will be crucial. A portfolio approach enables diagnostics providers to group those with similar collection history or reimbursement rates together.
Only XiFin® Empower RCM has the financial integrity and reporting tools laboratories need to deal with FASB 606.
XiFin’s financial underpinnings means it has been designed to comply with FASB-like requirements from day one. Written in a financial language and built to have full referential integrity, the solution balances every client to the penny, every month, and with the ability to track billed vs. the amount expected to be paid vs. actual amount paid, laboratories have at their disposal the information needed for analysis, auditing, and reporting. Included is a complete financial accounting package that delivers GAAP and Sarbanes-Oxley compliant financial data for the general ledger.
XiFin’s cloud-based Business Intelligence is built on a world-class infrastructure that is powerful enough to handle the demands of FASB and other reporting and analytical needs. XiFin BI provides at your fingertips the ability to drill down and slice and dice to deliver answers to the questions your accountants might pose. XiFin BI lets you see things like collection rates and collection history over time, aging, and trending, broken up by the classes and types that FASB dictates. Not only do XiFin laboratories understand their revenue in ways not possible with standard billing solutions, but they are able to deliver information that aids and speeds the accounting/auditing process immeasurably, and that acts as supporting evidence of revenue history.