Taking Flight with Audubon Audubon is a specialized CRO providing collaborative support for the submission of regulatory documents in markets around the world. Our highly experienced team comprises senior medical writers, project leads, and document managers with decades of industry experience. Our comprehensive service covers all aspects of regulatory writing, project management and production of quality submission-ready documents. We also support diverse therapeutic and disease areas, including dossiers for both CTD and non-CTD accepting markets. Whatever your needs, Audubon can help develop and implement submission communications strategies with the product label in mind, aligning key messages across critical clinical study reports and CTD summary modules. A deep understanding of regulations, and adherence to best practices, allows us to anticipate your needs, adjusting quickly to unexpected changes in demands, circumstances, and timelines. Moreover, we provide continuity and streamlined communications by dedicating one of our most experienced associates to act as your personal point of contact. Put simply, Audubon’s aim is to build a relationship with your team and to act as a direct extension of their talent and experience. With associates throughout North America and Europe, we offer the agility, accessibility, and skills you are looking for.
