Four trade associations have banded together to ask Congress to allocate an additional $5 million in funding to help the US Food and Drug Administration regulate dietary supplements.
Guardion Health Sciences Announces Appointment of Craig J Sheehan as Chief Commercial Officer streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.
Guardion Health Sciences Announces Appointment of Craig J. Sheehan as Chief Commercial Officer
Proven Leader of Viactiv Brand to Oversee Ramp Up and Commercial Activities at Guardion Guardion Health Sciences, Inc. San Diego, California, UNITED STATES
SAN DIEGO, June 03, 2021 (GLOBE NEWSWIRE) Guardion Health Sciences, Inc. (Nasdaq: GHSI) (“Guardion” or the “Company”), a clinical nutrition and diagnostics company that develops clinically supported nutrition, supplements, medical foods and medical devices, today announced the appointment of Craig J. Sheehan as its Chief Commercial Officer.
Mr. Sheehan joins Guardion following the Company’s recent acquisition of Activ Nutritional. Mr. Sheehan was the senior executive responsible for the Viactiv brand as a member of the executive leadership team of Adare Pharmaceuticals for the last four years. Prior to that position, Mr. Sheehan served in key marketing leadership positions at Church & Dwight, w
Trade groups slam DSHEA 2.0 proposal related to adverse events In this story, the Center for Science in the Public Interest and industry trade groups debate the merits of requiring manufacturers to report all adverse events associated with their dietary supplements. Also weighing in: a prominent Harvard Medical School professor who studies supplements, and an expert in adverse event management and regulatory compliance services.
Editor’s note: This is the third article in a series on proposed reforms to DSHEA by several consumer groups in a recent letter to Congress.
Some consumer advocacy groups want U.S. lawmakers to impose a new requirement that manufacturers of dietary supplements report to FDA all “adverse events” associated with their products.
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