Anita Kravitz

Director, Medical Writing
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Anita has over 14 years of experience providing consultative and regulatory medical writing services to the pharmaceutical industry. 

From Integrated clinical study reports (Phase I through Phase IV and PK/PD), protocols, INDs, NDA summaries (including ISS/ISE), investigator’s brochures, briefing packages, to various other regulatory submission documents compliant with FDA and ICH Guidelines.   Anita has earned a highly talented expertise in all aspects of writing and compilation of clinical and nonclinical sections of US and European regulatory submissions.

Anita has the proven ability to lead inSeption teams and manage project timelines for successful on-time delivery of regulatory and clinical documents, and has built a reputation over time with clients and colleagues based on a foundation of integrity and service.

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