NetworkNewsBreaks – Blackbriar Regulatory Services Announces Entry Into Medical Device Manufacturing
Sep 11, 2020
Blackbriar Regulatory Services (“BRS”), a firm specializing in helping small to mid-sized domestic and international companies navigate the regulatory landscape to bring their FDA regulated product concepts to market, today announced its entry into medical device manufacturing. According to the update, BRS has launched mask manufacturing operations to support U.S. demand for personal protective equipment (“PPE”) amidst the COVID-19 pandemic. “When BRS was created earlier this year, medical device manufacturing was part of our predetermined business strategy,” said BRS CEO Russ Rogers in the press release. “With the COVID-19 outbreak, it made sense to accelerate our plan to enter into this market segment, and we had the resources to quickly ramp up our manufacturing capabilities to help U.S. frontline workers with the domestic face mask shortage. Because this aligns so well with our strategy, we already have in place the management team with experience in the medical device space, as well as the requisite quality systems, facilities, and non-woven materials processing background to do this right and get it done quickly. It’s really a perfect fit for us and natural progression.”
To view the full press release, visit http://nnw.fm/xVdh6
About Blackbriar Regulatory Services
Since its inception, BRS has perfected processes in cost efficient manufacturing, analytical testing, regulatory compliance audits and filings, rigorous project management, packaging design, and product stewardship for customers in the United States, Europe and Asia. BRS prides itself on speed and flexibility, while never compromising quality or its customers’ confidential information. Learn more at www.bb-rs.com.
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