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BONESUPPORT CEO Emil Billbäck Shares Insights About Cerament G, the New Bone Void Filler Launching in the US

XTalks

BONESUPPORT received market authorization from the FDA for Cerament G, the first and only bone graft with antibiotic elution that is approved for the US market. BONESUPPORT has recently received market authorization from the US Food and Drug Administration (FDA) for Cerament G, its bone graft with antibiotic elution.

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Bougie Bakes Enters the Pet Treat Market with Their New Bougie Barks

XTalks

The Bougie Bark cookies are preservative-free and do not contain any fillers. Therefore, it’s only natural for companies to cater to this growing consumer market. There is exponential growth in the pet treat market and it is predicted to reach $72.6 In 2020, the pet treats global market made an estimated $21.4

Marketing 105
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How MALK Organics Is Leading the Plant-Based Milk Revolution

XTalks

Let’s explore MALK Organics’ history, its competitors and what sets it apart in a fiercely competitive market. Its recent internal Series B investment round , led by Benvolio Group and Rotor Capital, underlines the brand’s significant growth and market potential. billion by 2032.

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SweetLeaf Xylitol: A New Frontier in Natural Sweetening

XTalks

SweetLeaf Xylitol, the latest innovation from Wisdom Natural Brands, marks a significant development in the natural sweeteners market. SweetLeaf Xylitol is distinct because it contains pure xylitol without any additional fillers or additives, making it a perfect one-to-one substitute for sugar in cooking, baking and beverages.

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Some Talc Products Contain Asbestos: Study

The Pharma Data

30, 2020 – Nearly 15% of talc-based cosmetic products analyzed in a recent study contained asbestos. She noted that EWG’s online database has identified more than 2,000 personal care products that contain talc, including more than 1,000 loose or pressed powders that could pose an inhalation risk. MONDAY, Nov. based institute.

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Novartis signs new initial agreement with BioNTech to support fill and finish of the mRNA Pfizer-BioNTech COVID-19 vaccine

The Pharma Data

Novartis blazoned moment that it has inked an original agreement to work its manufacturing capacity and capabilities to address the COVID-19 epidemic by expanding its support of the filler and finish of the Pfizer-BioNTech COVID-19 vaccine. The specifics will be bared when we conclude specific agreements.

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New Section 804 Drug Import Rule Does Not Allow Foreign Versions of FDA-Approved Drugs

Pharmacy Checkers

A drug is considered “FDA-approved” when the FDA approves the drug application of a manufacturer to market that drug in the United States. A foreign version of an FDA-approved drug is a finished pharmaceutical that has the active ingredient contained in the FDA-approved version and is approved in another country.