In vitro diagnostic (IVD) and medical device research services including regulatory affairs and clinical trial management directed by industry experts. Independent CRO quality oversight, GCP auditing, CAPA management, GMP solutions and more to establish and uphold research quality and data integrity.
Proven staffing solutions for in vitro diagnostic, medical device and biopharmaceutical companies worldwide, supported by a global network of well-vetted professionals. Beaufort is an ISO 9001:2015 certified, global contract research organization that partners with in vitro diagnostic (IVD), medical device and biopharmaceutical developers to provide a full range of clinical, regulatory, quality and staffing solutions.
Proven staffing solutions for in vitro diagnostic, medical device and biopharmaceutical companies worldwide, supported by a global network of well-vetted professionals. Beaufort is an ISO 9001:2015 certified, global contract research organization that partners with in vitro diagnostic (IVD), medical device and biopharmaceutical developers to provide a full range of clinical, regulatory, quality and staffing solutions.
Services
Beaufort is an ISO 9001:2015 certified, global contract research organization that provides in vitro diagnostic, medical device and biopharmaceutical clinical and regulatory services, and a full range of quality solutions and staffing solutions. For more than a decade, in vitro diagnostic, medical device and biopharmaceutical companies worldwide have trusted Beaufort because of our client-oriented approach to research.
The leaders at Beaufort are highly skilled and educated professionals who provide successful project guidance time after time, and, therefore, many are esteemed as leaders in the greater industries we serve. Our management team has earned an exceptional reputation among the clients we've worked with worldwide.
With Beaufort, your research is directed by industry experts - we know how regulatory expectations are evolving for everything from companion diagnostics to laboratory developed tests and what those expectations mean for your intended outcomes. Our team manages clinical trials from start to finish and provides complete regulatory affairs support for even the most complex in vitro diagnostics, companion diagnostics and biomarkers.
Beaufort's clinical trial management services are supported by a highly qualified team of diagnostic and medical device experts. Our proven track record in managing both domestic and international clinical trials from beginning to end sets the foundation of a lineup of industry-leading services. We will fully manage and provide strategic assistance for every phase of your clinical trial.
A sound regulatory strategy sets the foundation for successful health care innovation. This is particularly relevant when developing medical devices including highly sophisticated In Vitro Diagnostic (IVD) products, as well as Laboratory Developed Tests (LTDs), individualized medicines and traditional medical devices that face increased oversight and evolving regulations.
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