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TDD Industry News and Views: Weekly Updates on Comings, Goings, and Other Happenings in Dermatology

The Dermatology Digest

The two companies will collaborate in sales, marketing, education, and research. market share within three years. market,” says Ethan Min, CEO of BENEV, in a news release. .” market,” says Ethan Min, CEO of BENEV, in a news release. “We Hugel Inc.’s s botulinum toxin product Letybo is coming to the U.S.

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Oh, The Places Dermatology Will Go in 2024!

The Dermatology Digest

The Dermatology Digest asked key thought leaders and editorial advisory board members to take out their crystal balls and weigh in on what’s to come in 2024 and beyond. It has great efficacy and safety and is oral… [This means] no shot and no risk of anaphylaxis.” We will, for sure, have new medications for chronic urticaria.”

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PHysicians & the esthetician

Southeastern Esthetics Institute

Having a thorough understanding of the dermatology and plastic surgery procedures, in addition to all new and modern cosmetic procedures on the market, is critical in assisting your clients in answering questions. Having daily and weekly communication when dealing with patients receiving treatment is critical.

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If Fragrance In Skincare Scares You, Read This

Renee Rouleau

Learn more about the different marketing terms used in skin care and what they really mean. People tend to assume natural fragrances are better than synthetic ones, but I think a lot of this has to do with the increased popularity of “clean” beauty marketing. What is Fragrance? The short answer is no.

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FDA Green Lights New Stelara Biosimilar

The Dermatology Digest

Market Access at Teva, in a news release. Bringing Selarsdi to market in the U.S. The post FDA Green Lights New Stelara Biosimilar appeared first on The Dermatology Digest. says Thomas Rainey, Senior Vice President, U.S. Robert Wessman, Chairman and CEO of Alvotech, adds, “.

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FDA, EMA Accept Galderma’s BLA for Nemolizumab for PN and AD

The Dermatology Digest

In addition, the European Medicines Agency has also accepted the Marketing Authorization Applications for nemolizumab in prurigo nodularis and atopic dermatitis. The European Medicines Agency has also accepted Galderma’s Marketing Authorization Applications for nemolizumab in both prurigo nodularis and atopic dermatitis.

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MHRA Grants Marketing Authorization for LEO Pharma’s CHE Cream in Great Britain

The Dermatology Digest

The Medicines and Healthcare Products Regulatory Agency (MHRA) has granted marketing authorization in Great Britain for delgocitinib cream (Anzupgo, Leo Pharma) for the treatment of adult patients with moderate to severe chronic hand eczema (CHE), for whom topical corticosteroids are inadequate or inappropriate.