Mark A. Mannebach

Mark Mannebach has over 30 years of experience in the pharmaceutical industry in Regulatory Affairs with extensive knowledge of Quality Assurance, Program Management, and Pharmaceutical Science. During his career, he has filed numerous NDA’s, BLA’s, PME’s, ANDA’s and 505(b)(2) submissions. Mark has assisted with the development of branded and specialty pharmaceuticals as well as biologics for many therapeutic applications including ophthalmology, pain management, neurology/CNS, and anti-inflammation.