Do you know, for investors, every new project or substance is an opportunity to expand their chances of success? Like other industries, the health and wellness industry is also experiencing tectonic shifts. The shifts appear when underground drops are thrust up into the mainstream. Every new addition to the market landscape becomes a potential win-win for investors. The investors know their benefits will lure in customers, whether CBD or other botanicals. Therefore, investing is always good when the market is small and you know it will increase threefold. This time too, a new substance has surfaced to attention: Kratom, and we can use the best Kratom strain for energy.
Tag: Food and Drug Administration
Federal Judge Orders FDA to Speedup Release of Pfizer Vaccine Data
the staff of the Ridgewood blog
Fort Worth Tx, on Thursday a federal judge in Texas ordered the Food and Drug Administration to make public the data it relied on to license Pfizer’s COVID-19 vaccine, imposing a dramatically accelerated schedule that should result in the release of all information within about eight months.
Continue reading Federal Judge Orders FDA to Speedup Release of Pfizer Vaccine Data
Dr. Fauci says all three Covid vaccines highly effective, urges people to take shot most available
the staff of the Ridgewood blog
Washington DC, the White House Chief Medical Advisor Dr. Anthony Fauci said on Sunday he would take the newly approved Johnson & Johnson Covid-19 vaccine and urged Americans to take whichever shot is available when they are eligible.
How CBD and THC Can Improve Your Life
In modern times, it seems everyone has an understanding of what is good for their body. Eating healthy, constantly staying active, and taking natural supplements helps boost the immune and circulatory system but very few people take into consideration their mental health.
Garrett Calls on FDA to Answer Questions About EpiPen Monopoly
September 24,2016
the staff of the Ridgewood bog
Ridgewood NJ, Rep. Scott Garrett (NJ-05) called on the Food and Drug Administration (FDA) to express concerns over the near monopoly currently held by Mylan Pharmaceuticals on the EpiPen (epinephrine injection) which is used in the treatment of severe allergic reactions. The price of these life-saving devices has skyrocketed recently, making them unaffordable for many Americans families.
“Like many government bureaucracies, the Food and Drug Administration stifles innovation and creates unnecessary roadblocks that end up hurting the American people,” said Garrett. “In this case, their short-sightedness has made a common treatment that millions of Americans rely on prohibitively expensive. The FDA has a job to protect Americans and ensure the food and drugs we use are safe, but they also need to make sure their actions don’t hurt the very people they’re trying to protect.”
The letter, signed by a number of Members of Congress, asks the EPA to allow other companies to make alternatives to the EpiPen product by streamlining the FDA review process. Specifically, the letter asks:
– If the FDA can clarify whether any barriers exist to the approval of safe alternative products to EpiPens.
– How many alternatives to Mylan’s EpiPen are currently being reviewed by the FDA
– Where these alternatives are in the review process
To read the entire letter, click here.