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IBN (InvestorBrandNetwork) Announces Latest Episode of The Bell2Bell Podcast Featuring Dr. Faz Chowdhury, CEO of Nemaura Medical Inc.

IBN (InvestorBrandNetwork) Announces Latest Episode of The Bell2Bell Podcast Featuring Dr. Faz Chowdhury, CEO of Nemaura Medical Inc.
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"Buzz on the Street" Show: Nemaura Medical (NASDAQ: NMRD) Granted UK Trademark "Meta Score"

"Buzz on the Street" Show: Nemaura Medical (NASDAQ: NMRD) Granted UK Trademark "Meta Score"
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Breaking News: Nemaura Medical Granted UK Trademark "Meta Score," a Digital Biomarker Term for its Metabolic Health Program

Breaking News: Nemaura Medical Granted UK Trademark "Meta Score," a Digital Biomarker Term for its Metabolic Health Program
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Form 8-K Nemaura Medical Inc. For: Jun 30

Form 8-K Nemaura Medical Inc. For: Jun 30
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Fostering medical device improvement

The Voluntary Improvement Program (VIP), through the Medical Device Innovation Consortium (MDIC), evaluates the capability and performance of a medical device manufacturer’s practices using third-party appraisals.

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FDA Draft Guidance for Fostering Medical Device Improvement Using the Voluntary Improvement Program | Knobbe Martens

On May 5, 2022, the FDA’s Center for Devices and Radiological Health (CDRH) issued draft guidance regarding the FDA’s Voluntary Improvement Program (“VIP”). The draft guidance,...

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Voluntary Improvement Program (VIP) Becomes the First Case for Quality Program Recognized by the FDA

FDA highlights key opportunities offered by VIP, which leverages ISACA’s Medical Device Discovery Appraisal Program (MDDAP)SCHAUMBURG, Ill.--(BUSINESS WIRE)--The Voluntary Improvement Program (VIP) has become the first Case for Quality program recognized by the United States Food and Drug Administration (FDA) throug...

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Stock Market | FinancialContent Business Page

Stock Market | FinancialContent Business Page
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Nemaura Medical to Present at the Maxim Group 2022 Virtual

Loughborough, England, March 24, 2022 (GLOBE NEWSWIRE) -- Nemaura Medical, Inc. (NASDAQ: NMRD), a medical technology company focused on developing and...

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Don't Go Changing . . . Unless You Ask FDA | Arnall Golden Gregory LLP

The Food and Drug Administration recently issued a Warning Letter to a medical device manufacturer for making significant changes to its 510(k)-cleared products for uses outside the...

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