*Martika is not licensed to practice law. Her activities are directly supervised by members of the firm licensed to practice law in the firm’s Winston-Salem office.

As a regulatory research analyst, Martika uses her scientific background and clinical research experience to guide clients in navigating the US Food and Drug Administration’s (FDA) regulatory pathways.

Martika is an integral part of Womble Bond Dickinson’s in-house Regulatory Affairs team. She has experience preparing regulatory submissions to FDA for drugs, biologics, and medical devices including: Investigational New Drug applications, Investigational Device Exemption applications and meeting requests. 

She is also familiar with registering and reporting study results in ClinicalTrials.gov and is able to advise clients on compliance issues related to the site.   

Before joining Womble Bond Dickinson, Martika worked as a research regulatory specialist in clinical and translational research at Wake Forest Baptist Medical Center. She also has experience with reviewing clinical study protocols.