Monday, January 30, 2023

Tag: FDA regulation

The Minds of Men: A Stunning New Film About Covert Mind...

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The importance of a remarkable new film, The Minds of Men, was underscored by otherwise inexplicable recent events surrounding government support of ECT. Without any testing or opportunity for public response, effective December 26 the FDA has approved ECT for infliction upon people with “treatment-resistant depression.”

Most Direct-to-Consumer Drug Advertisements Do Not Adhere to FDA Guidelines

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Few DTC drug advertisements fully adhere to FDA guidelines, the overall quality of information provided in DTC advertisements is low, and some advertisements market off-label indications.

We Pay a High Price for Unregulated Medical Devices

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From The Lown Institute: New investigations and research are beginning to show the dangerous consequences resulting from the FDA's lack of oversight of medical devices. "It sounds crazy...

Comments by Shock Survivors and Their Loved Ones

The #FDAStopTheShockDevice petition has received over 2,200 signatures and 800+ comments. A more thorough analysis of those comments is forthcoming, however, we wanted to offer a glimpse of what people shared. The sixth, seventh, and eighth most common words used in the comments submitted through the petition were "damage," "barbaric" and "torture." We must continue the fight to make sure that the FDA hears the people who will be adversely affected by the proposed rule if it becomes an order. There is still a small window of time for you to sign the petition and leave a comment to the FDA.

Only 72 Hours Left to Say #FDAStopTheShockDevice

As part of the effort to stop the down-classification of the shock device, on March 24, 2016, people who are psychiatric survivors, shock survivors, allies, and MindFreedom International members sent a 47-page public complaint to the FDA Ombudsman Office and Medical Devices Ombudsman concerning the FDA's attempts at down-classifying the shock device. Here are some excerpts. Please sign the petition and add your support to our growing strength!

40 Days to Tell the #FDAStoptheShockDevice

Please join us in demanding that the FDA stop the shock device from being down-classified to a Class II device. We have until March 28th, 2016.

“F.D.A. Targets Inaccurate Medical Tests, Citing Dangers and Costs”

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Following an eye-opening FDA report, the Obama administration is attempting to pass tighter regulations on medical tests. “Inaccurate and unreliable medical tests are prompting...