Enforcing Financial Reporting Standards: The Case of White ...
Enforcing Financial Reporting Standards: The Case of White ...
Enforcing Financial Reporting Standards: The Case of White ...
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we acquire R&D, that’s a different story. In that case, we follow SFAS No. 141 and SFAS<br />
No. 142 and capitalize the acquired in-process R&D. But I’m not really sure what I would do<br />
in your situation. Besides, you’re an IFRS guy and, as far as I know, R&D accounting still<br />
differs on our continents.” Peter didn’t feel like his American counterpart had fully<br />
understood his problem but was still thankful for Jeff’s quick assessment <strong>of</strong> the situation.<br />
Feeling that he had to solve the issue himself, Peter considered the nature <strong>of</strong> the<br />
upfront compensation. <strong>White</strong> Pharmaceuticals AG conducted the payment to pr<strong>of</strong>it from the<br />
research carried out by Neurocentral, Inc. While <strong>White</strong> Pharmaceuticals AG received all<br />
rights to the research performed, Peter did not perceive the five million Euros as an<br />
acquisition <strong>of</strong> an intangible asset. Instead, he felt that <strong>White</strong> only provided Neurocentral with<br />
the funding for research activities that the company performed. Following this reasoning, the<br />
payment had to be regarded as if <strong>White</strong>’s researchers were conducting the research. And,<br />
considering the status the research was in at that time, no one could tell if the project would<br />
eventually yield a product that <strong>White</strong> would be able to sell. <strong>The</strong>refore, the up-front payment<br />
would fall under the definition <strong>of</strong> research expenditure which IAS 38 prohibits from<br />
capitalizing. Although being skeptical <strong>of</strong> his argumentation, he charged the five million Euros<br />
to <strong>White</strong>’s R&D expenses.<br />
<strong>The</strong>reafter, the project proceeded as expected and Neurocentral, Inc. started the<br />
clinical studies in 2002. In the same year, they were able to complete the first phase <strong>of</strong> the<br />
studies which provided them with a safety pr<strong>of</strong>ile <strong>of</strong> the transdermal patch. Acting upon their<br />
role in the collaboration agreement, <strong>White</strong> transferred the first milestone payment <strong>of</strong> ten<br />
million Euros as soon as they received the latest research report from their partner. As a<br />
consequence <strong>of</strong> the payment, Peter was again confronted with the accounting for the alliance.<br />
Considering that the project had progressed to the development phase which, according to<br />
IAS 38, meant that incurred costs should be recognized, he wanted to discuss a possible<br />
5