Beaufort’s commitment to a quality-first approach as an ISO 9001:2015 certified company coupled with our deep experience in guiding research has formed the basis for innovative quality services. With independent CRO quality oversight, Good Clinical Practice (GCP) auditing solutions, Corrective and Preventive Actions (CAPA) management and more, we’ll help you design, optimize and review processes to ensure your clinical program adheres to the most stringent regulatory guidelines and expectations.
Our quality and compliance experts will help you satisfy increasing global regulatory agency demand for trial management supervision and ensure you maintain uninterrupted operations. In addition, we offer auditing, training, Standard Operating Procedure (SOP) development and other quality and compliance services for all GxP standards, as well as support for regulatory agencies around the world.
When you need to ensure the conformance, control and continuous improvement of your program activities, trust Beaufort. We have in-depth experience with quality management systems, including audits and compliance analysis, development, implementation and validation. Our operations span the globe, encompassing regulatory requirements in North America, Europe, South America and Asia-Paciﬁc.
Read case studies of how Beaufort has helped clients meet their Quality needs.