Doug Ferguson

Doug Ferguson has extensive experience in the field of regulatory affairs and clinical and regulatory affairs. Doug is currently serving as the Vice President of Clinical and Regulatory Affairs at Beta Bionics since June 2021. Prior to this, they founded Metrowest Regulatory Associates, LLC in August 2019. Additionally, Doug has worked as an Adjunct Professor of Biomedical Engineering at Worcester Polytechnic Institute since August 2020.

In terms of previous roles, Doug has held various positions at Tryton Medical, including VP of Regulatory, Quality, and Clinical from April 2017 to September 2019, VP of Regulatory and Quality from 2011 to 2018, and VP of Regulatory and Clinical from 2008 to 2011.

Before their time at Tryton Medical, Doug worked at BD as the WW Director of Regulatory Affairs from 2006 to 2008. Doug also held managerial and directorial positions at Boston Scientific Corporation from 2000 to 2006.

Earlier in their career, Doug served as the Regulatory Affairs Manager at Vasca from 1998 to 2000, and as a Regulatory Affairs Specialist at C.R. Bard from 1994 to 1998. Doug began their career as a Quality Regulatory Manager/Sr. Scientist at Spire Corporation in 1991.

Throughout their career, Doug Ferguson has consistently demonstrated expertise in regulatory affairs and has gained extensive knowledge in the field.

Doug Ferguson earned a Bachelor of Science (BS) degree in Biomedical Engineering and Materials Science and Engineering from The Johns Hopkins University. Doug attended this institution from 1985 to 1989. Following that, they pursued a Master of Science (MS) degree in Biomedical Engineering at the University of Alabama at Birmingham from 1989 to 1991. In September 2020, Doug obtained the Regulatory Affairs Certification (RAC-US) from the Regulatory Affairs Certification Program.