Eeke Romo, DSc is a Dutch-trained physician with extensive experience in design and conduct of experimental research studies in an academic environment as well as clinical trials in support of product registration. She has more than 25 years of experience in industry at Baxter Healthcare, Edwards Division, Theracardia, a venture-backed private company, and numerous other companies in the capacity of a Clinical Research Consultant and Medical Writer. Dr. Romo’s skills and expertise include preparation of clinical, pre-clinical, annual and interim reports for PMA, IDE and IND submissions; development of protocols, CRFs, manuals, training material for devices, pharmaceuticals, biologics and drug studies; extensive literature reviews for regulatory submissions; preparation of manuscripts for submission to peer-reviewed journals; and management of clinical trial execution. She has prepared final clinical reports for at least 8 original PMA submissions.
Regulatory Pathways Group Inc.
a California corporation
Inquiries and general information:
info@regulatorypathways.com
© Regulatory Pathways, Inc. • All rights reserved • Last updated February Year
Site Developed by Human Powered Design