My experience is in crafting clinical and regulatory submissions in the medical device and pharmaceutical industries. When you work with me, your submission stakeholders, both external and internal, will thank you for the clarity of the final document product as well as the efficiency of the submission development process. I have a history of combining my experience and insight from diverse technical fields with my knowledge of regulations, guidances, and best practices in medical writing to ensure that your organization’s research is appropriately contextualized and clearly communicated. My focus on clear writing ensures that your painstaking efforts in doing transformative science are not lost while navigating complex clinical and regulatory interactions.
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