Do new revenue recognition rules smooth out life science and biotech wrinkles?
October 30th, 2009 by Pam SintrosEarlier this month we wrote about how the new revenue recognition rules are having an impact in the technology sector, but it doesn’t end there. In fact, my colleague Michelle Kupka and I will be leading a webcast regarding the current changes in revenue recognition this coming Tuesday, November 3. And if there are readers out there who have struggled with rev rec, we’d love to hear your take on whether the new rules will be an improvement - or just another hurdle.
Among the industries that will be affected, life sciences and biotech stand out due to their long R&D cycles, their capital requirements and the infrastructure required to manage and market products from concept to distribution. This hits home for us in Massachusetts, where the steady growth of the life science and biotech industries depend not just on science and commercialization, but on compliance and a strong balance sheet as well.
A great number of life science and biotech projects are embarked upon as joint development arrangements with pharmaceutical companies or distributors, and as a result, revenue is often generated under complex scenarios. These arrangements often include payments linked to milestones, upfront payments, joint funding payments, joint product launch funding, licensing of future products developed and other issues. It is these complicated relationships that result in misstated revenue, in turn leading to an above-average rate of financial accounting restatements.
FASB’s new revenue recognition rules take these circumstances under consideration, and in particular they address:
1. whether the arrangement represents a single unit of accounting or multiple units;
2. if the arrangement represents a single unit of accounting, how the revenue should be recognized when such arrangements spans over multiple financial reporting periods; or
3. if there are multiple units, how revenue should be attributed.
Under the new revenue recognition guidance, the elimination of the requirement to establish fair value of undelivered products or services using objective and reliable evidence (replaced by the concept of “Estimated Selling Price”), as well as the elimination of the use of the residual method for allocating arrangement consideration will make things a bit easier and serve to facilitate consistency in revenue recognition accounting for these types of collaborative development arrangements.
While we will begin to see some clarity, vagueness will still persist in certain areas. On the bright side, due to the life science and biotech industries’ unique approach to collaborative development arrangements and long-term view of success, companies should find some comfort in these new rules.
