Our industry is constantly evolving, from in vitro diagnostic (IVD) advances to regulatory requirements to clinical trial best practices. Get an expert perspective from Beaufort.
Beaufort Maintains its Commitment to Quality with Successful ISO 9001:2015 Recertification … Read more
Promega Corporation, a global leader in providing innovative products and solutions to the life sciences industry, has received FDA … Read more
Abbott Receives FDA Emergency Use Authorization for Breakthrough COVID-19 Tests. … Read more
As we move closer to the May 2022 deadline where all IVD products marketed in the … Read more
Conducting Monitoring Visits Remotely for IVD Clinical Trials During the COVID-19 Pandemic … Read more
Beaufort CRO is closely monitoring the evolving circumstances surrounding COVID-19, including review of the latest state, national and international … Read more