Beaufort’s commitment to being quality-first is exemplified by our status as an ISO 9001:2015 certified company. This, and our deep experience in guiding research, forms the basis for our innovative quality services. With comprehensive quality management, Good Clinical Practice (GCP) auditing, and Good Manufacturing Practice (GMP) quality solutions, we’ll help you design, optimize and review processes to ensure that 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 demands for trial management supervision and 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 working with regulatory agencies around the world.
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 the Asia-Paciﬁc.
Read case studies of how Beaufort has helped clients meet their Quality needs.