Beaufort CRO (www.beaufortcro.com) is a global contract research organization (CRO) that provides in vitro diagnostic (IVD), ... medical device and biopharmaceutical companies with a full range of clinical, regulatory, quality and staffing solutions. For over 15 years, we have earned a reputation for successfully helping sponsors get their products to market -- on time and on budget. Our depth of experience and proven track record means we can apply the highest level of expertise across every step of the process from project inception through regulatory submission. Most importantly, our dedicated and specialized teams develop solutions that truly reflect your unique project needs or gaps, including: • Clinical Trial Services: Efficient trial management, site selection, monitoring, data management and biostatistics • Regulatory Affairs: Result-focused regulatory strategies, protocol development, and pre- and post-market submissions and support • Quality Solutions: Comprehensive on-site gap assessments, auditing support and remediation services In addition to being one of the only CRO’s that is ISO 9001:2015 certified, Beaufort’s experience with hundreds of clinical trials and regulatory submissions helps ensure that you have a qualified partner by your side. Our teams are also experts in working across a wide range of platforms, therapeutic areas, regulatory pathways and technologies. See how Beaufort CRO can accelerate your medical innovation -- and put our experience to work for you. info@beaufortCRO.com 757-383-6000 read more