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HART member producers of 7-OH adopt GMP standards, third-party testing, and child-resistant packaging to further ensure ...
The U.S. Food and Drug Administration (FDA) plans to update the standard of identity for canned tuna, as well as its standard ...
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Inquirer.net on MSNPharma, drug store owners to DTI: No to sari-sari stores selling medsThe proposal of the Department of Trade and Industry (DTI) to authorize sari-sari stores to sell over-the-counter (OTC) drugs ...
The steady erosion of experienced staff is slowly compromising FDA work and low morale is pushing more workers to the exits ...
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FDA creates task force to enhance medical devices regulation - MSNThe Food and Drug Administration (FDA) has formed a task force assigned to improve regulation of medical devices in the country. The Task Force Obsidian was established to help stakeholders ...
Regular regulation: Agencies like the EPA and FDA do more than the public sees - New York Daily News
This week, the Environmental Protection Agency moved to largely ban the use of trichloroethylene and tetrachloroethylene, known as TCE and Perc, respectively, in most consumer and commercial uses. … ...
Layoffs at the FDA, USDA and CDC could erode the U.S. food safety system. Experts aren’t so worried about milk or chicken today; they’re concerned about the future.
General Food Labeling Requirements and Labeling-Related Sample Analysis — Domestic and Import” replaces the previous 2010 ...
The FDA’s regulation had proposed a multiyear timeline that would have phased in reviews and other requirements for LDTs through 2028—while offering exemptions for tests manufactured and ...
In the commitment to safeguarding public health and enforcing strict regulatory standards, the Food and Drug Administration (FDA) has established Task Force Obsidian—a Technical Working Group (TWG) ...
In the absence of meaningful regulation from the FDA, the supplement industry will no doubt take RFK Jr.’s stance as a free pass. Skip to Main Content Manage alerts for this article ...
In 1970, the FDA removed it from the "GRAS" list after multiple toxicity studies by the Canadian Food and Drug Directorate in 1969, according to the CSPI. On July 3, the FDA revoked the regulation ...
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