“…If market access is granted, manufacturers get a limited time-in most cases, 20 years as of initial application filing, 10-12 of which are typically spent in clinical development-of market exclusivity, after which generic therapies can enter the market. Life sciences firms' marketing efforts are typically capped (e.g., in many European countries) and/or regulated (e.g., some states in the United States require medical sales representatives to undergo a Because of its vast importance and unique challenges, the marketing literature has recently turned to the life sciences industry to study sales force effectiveness (Manchanda and Chintagunta 2004; Manchanda and Honka 2005;Manchanda, Rossi, and Chintagunta 2004;Mizik and Jacobson 2004;Venkataraman and Stremersch 2007), therapy compliance (Bowman, Heilman, and Seetharaman 2004;Wosinska 2005), communication effectiveness (Cleanthous 2004;Iizuka and Jin 2005;Macias and Lewis 2003;Mukherji, Dutta, and Rajiv 2004;Wosinska 2006), and innovation (Chandy et al 2006;Ding and Eliashberg 2002;Prabhu, Chandy, and Ellis 2005;Sorescu, Chandy, andPrabhu 2003, 2007;Wuyts, Dutta, and Stremersch 2004), among other areas.…”