Ms. Anne F. McKay has been Regulatory Consultant at Fennec Pharmaceuticals Inc. (formerly, Adherex Technologies Inc.) since May 2010. Ms. McKay's primary responsibility is to develop and implement Adherex regulatory strategies. She served as Vice President of Regulatory Affairs at Ocera Therapeutics, Inc. since January 2014 until April 28, 2016. She served as Vice President of Regulatory Affairs at Biolex Therapeutics Inc. (formerly, Biolex Inc.) since November 2008. She was responsible for the development and implementation of Biolex's regulatory strategies. Ms. McKay worked as a Consultant with BWA Consulting LLC, providing regulatory and compliance guidance to a number of biotech and pharmaceutical companies. She served as an Executive Vice President - Drug Regulatory Affairs of Triangle Pharmaceuticals Inc., since October 2000, and served as Vice President, Drug Regulatory Affairs from October 1996 to September 2000. Ms. McKay served as the Director of Regulatory Affairs of Medco Research Inc. Ms. McKay served as the Director of Regulatory Affairs, North America, and held various other regulatory positions during a 15-year tenure at Burroughs Wellcome Co. Her department was responsible for providing support for various FDA submissions, including the NDA submissions for AZT and acyclovir. Ms. McKay holds a B.S. in Animal Science from Michigan State University.