Nanita Cranford

Ms. Cranford has been Director of Regulatory Affairs for Jazz Pharmaceuticals since August 2012 and is fortunate to be part of a dynamic and growing team enjoying rapid change.

She has more than 20 years of experience in writing and publishing, with the last 12 being in the pharmaceutical industry in regulatory affairs. Her experience includes overseeing 1,500 in-house eCTDs submissions – including creating submissions without specialized eCTD software in her first regulatory publishing position at InterMune.