Pharma in Brief

NOVEMBER 20, 2023

In recent months, the Federal Courts have twice upheld Health Canada’s findings as to what is, and is not, a natural health product. The Courts’ decisions provide insight into how natural health products are distinguished, under federal law, from cosmetics and from drugs subject to the Food and Drug Regulations.

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Scienmag

OCTOBER 29, 2020

Pharmacy faculty member studies properties that are environmentally friendly Credit: University of Cincinnati University of Cincinnati cosmetic scientist Harshita Kumari has received a research grant for more than $700,000 for a multi-year study to explore certain new proprietary surfactants for industrial applications and personal care products such (..)

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XTalks

APRIL 14, 2021

Scientists used synthetic biology and computational protein design tools to develop an enzymatic process to transform red cabbage anthocyanins into their desired color. This process has been used in the food industry before, such as in cheese production, for example. How Are Synthetic Food Dyes Regulated?

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pharmaphorum

DECEMBER 9, 2021

Heather Barnes, external innovation lead EMEA at Johnson and Johnson Consumer Health, is a scientist who is truly passionate about consumer health. I am fascinated by the breadth of my role, which encompasses self-care products, skin health, sustainability and much more. From the very beginning, I thought, ‘Right, I love this!

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XTalks

DECEMBER 10, 2020

Funded by EIT Food , the Digital Marketplace for Side Streams will help food companies upcycle waste to produce by-products by matching them with businesses that have an overabundance of food. The goal of the marketplace is to inspire more companies to consider ways they can reduce waste from food production.

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XTalks

NOVEMBER 24, 2022

Earlier this week, the US Food and Drug Administration (FDA) sent out warning letters to five companies illegally selling CBD-infused food and beverage products. According to the warning letters, these products are considered adulterated under “section 402(a)(2)(C)(i) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act), 21 U.S.C.

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FDA Law Blog

FEBRUARY 2, 2023

In our experience, FDA is inherently an empirically driven body of scientists, physicians, and policy-makers. For more on FDORA’s other provisions, see HPM’s complete summary here ). 42 U.S.C. § 262(k)(2)(A)(i)(I). 42 U.S.C. § 262(k)(2)(A)(i)(I).

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XTalks

NOVEMBER 7, 2023

Medical science liaisons play a pivotal role in disseminating knowledge about products, services and research findings. They are key in clarifying the optimal use of products, fostering scientific and medical dialogue among their colleagues and peers and serving as a vital resource for the medical community at large.

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Pharmacy Checkers

NOVEMBER 21, 2019

Wikipedia has an extremely long page aptly called Criticism of the Food and Drug Administration , much of it having to do with its role with prescription drugs, and less so other sectors, such as food, tobacco and cosmetics. . billion, about 50% was dedicated to regulating medical products, including prescription drugs. Far from it.

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The Pharma Data

NOVEMBER 30, 2020

30, 2020 – Nearly 15% of talc-based cosmetic products analyzed in a recent study contained asbestos. Environmental Working Group (EWG) — an American advocacy nonprofit that commissioned the tests and did the analysis — said methods used by the cosmetics industry to screen talc supplies are inadequate. MONDAY, Nov.

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The Pharma Data

APRIL 7, 2023

The decision was issued jointly by the FDA Commissioner and Chief Scientist. Following the hearing, the FDA Commissioner and Chief Scientist reviewed the record for this matter, including the submissions by CDER and sponsor Covis Pharma, public comments to the docket , the transcript of the hearing and the Presiding Officer’s report.

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The Pharma Data

DECEMBER 18, 2020

Action Follows Thorough Evaluation of Available Safety, Effectiveness, and Manufacturing Quality Information by FDA Career Scientists, Input from Independent Experts. If the product meets the effectiveness standard and the benefit-risk assessment is favorable, the product is made available during the emergency.

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XTalks

AUGUST 2, 2023

Most of the company’s revenue comes from the manufacture and sale of biopharmaceutical products. They are committed to capitalizing on growth opportunities primarily through the advancement of their own product pipeline and constantly improving their existing products, as well as through business development activities.

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XTalks

FEBRUARY 26, 2021

He developed hundreds of products using peanuts, as well as sweet potatoes and soybeans. He worked with renowned fungal scientist (mycologist) L.H. Despite his testimony getting off to a rough start, Carver went on to describe the wide range of products that could be made from peanuts.

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FDA Law Blog

NOVEMBER 8, 2022

Last month, we advised planning for the end of the Covid-19 public health emergency (PHE) and highlighted that transition plans for Covid-19 products are amongst CDRH FY2023 priorities. In closing, he advised manufacturers who plan to market their products beyond the public health emergency to plan to submit marketing applications.

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