英文摘要 |
The President Obama of United States signed the Biologics Price Competition and Innovation Act of 2009 (BPCI Act) into law on October 23rd, 2010, and initiated the official regulation of biosimilar by the largest single pharmaceutical market in the world. From the perspective of patent or competition, biosimilar is similar to generics, because it references to a specific approved product as well. Likewise, whether there is patent or exclusivity covered the reference product is an issue to be considered in approving a biosimilar. However, from the perspective of technical nature, biosimilar and generics are totally different, because the structures of biologics are so complicated that different products can only be proved similarity or comparability, but not sameness, which is the prerequisite of the abbreviated approach in approving generics. In the budget of the U.S. government for fiscal year 2012, Obama administration proposed to reduce the 12 years of exclusivity for biologics to 7 years to control governmental expenditure. After the U.S. Food and Drug Administration published relevant guidelines for Biosimilar, Abbott Laboratories, one of the innovators of biologics, opposed the execution of BPCI Act. As the patents covered the biologics launched in 90’s expiring, the regulation of biosimilar is gaining attention. This article advocates the BPCI Act was fostered in a particular American political environment which does not exist in Taiwan. The regulatory policy of Taiwan shall echo not only the evolving technical nature, but also the industrial circumstances faced by Taiwan. |