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Jonathan Emord appears on Coast to Coast AM with George Noory

Jonathan Emord appeared for two hours on the nationally syndicated radio program “Coast to Coast” with George Noory on September 9, 2019 from 9PM to Midnight Pacific.  Jonathan discussed the opioid crisis, FDA complicity in the acts of major pharmaceutical companies in promotions that caused it, Trump’s efforts to stem the crisis, the Oklahoma public […]

PRESS RELEASE: Jonathan Emord Goes Round Two with the FDA on Electroshock Devices

For Immediate Release:  23 August 2017 Contact:  Dr. Linda Lagemann, Liaison to the Petitioners (415-640-7343)   Attorney Jonathan Emord and his co-counsel Kendrick Moxon have filed a Supplement to their Citizen Petition of August 2016, protesting the FDA’s Proposed Order to reclassify and make more readily available the Electroconvulsive Therapy (ECT) Device used to give […]

Jonathan Emord, “The FDA’s bow to barbarism” (Washington Times, Oct. 12, 2016)

Read Jonathan Emord’s October 12, 2016 article in the Washington Times concerning the FDA’s untenable decision to downgrade Electroconvulsive Therapy (ECT) medical devices from Class III to Class II: The FDA’s bow to barbarism:  Downgrading the brain injury risks from shock therapy is unjustified (Oct. 12, 2016) (opens in new window)

PRESS RELEASE: Attorney Jonathan Emord Takes on the FDA Over Electroshock (ECT) Device

For Immediate Release Contact:  Dr. Linda Lagemann 415-640-7343 Email:  2DrLagemann@gmail.com Attorney Jonathan Emord Takes on the FDA Over Electroshock (ECT) Device  In December 2015, the FDA issued a proposed order to down-classify the device used to deliver electroshock therapy. Today, Attorney Jonathan Emord filed a Citizens Petition with the FDA on behalf of 5 individuals […]

Proposed Federal Bill Would Prevent States, FDA, And Anyone Else From Informing Consumers Whether Food Is Bioengineered

  By Eric Awerbuch In April, 2014, five members of Congress introduced a bill, H.R. 4432 (hereinafter “the Bill”) seeking to regulate, among other things, the labeling of bio-engineered food products.[i]  The Bill, also known as the “Safe and Accurate Food Labeling Act of 2014,” is remarkable in that it:  1) prohibits the States from […]

Emord Interview in Freedom From Choice to Appear on the Stossel Show

Tim Delmastro, the director and co-producer of Freedom From Choice, winner of the Best International Documentary award, will be interviewed tomorrow night on the Stossel Show about his feature-length film. Freedom From Choice investigates the loss of our liberties.  It asks whether our daily choices, from what we eat to what we read, are in […]

FDA Requests Nominations for Drug Compounding List

President Obama signed the Drug Quality and Security Act (“DQSA”) into law on November 27, 2013.  The DQSA contained provisions concerning the oversight of human drug compounding.   For instance, it removed provisions of section 503A of the federal Food, Drug, and Cosmetic Act (“FDCA”) that the U.S. Supreme Court previously held were unconstitutional, thereby ensuring […]

Experts Recap Oral Arguments Before the Supreme Court in POM v. Coke

Oral arguments concluded on Monday, April 21, 2014,  in the POM v. Coke (Dkt. No. 12-761) case pending before the United States Supreme Court.  Click here to read what experts had to say about the arguments.  To recap, POM originally challenged Coke’s marketing for Minute Maid “Pomegranate Blueberry” fruit juice blend.  POM filed a Lanham Act […]

Attorney Bethany R. Kennedy Comments on NDI Notifications

In a recent article appearing on NutraIngredients-USA.com, Emord & Associates’ associate Bethany R. Kennedy comments on new dietary ingredient notifications for products that are approved drugs outside of the U.S.  Click below to read the full text of the article at NutraIngredients-USA.com. Hank Schultz, “Companies must walk fine line when bringing a supplement to market […]


Whether evaluating a concept, performing regulatory due diligence, maintaining or prosecuting regulatory filings, or contesting adverse litigation, Emord & Associates provides exceptional counsel for all your litigation and regulatory needs.

Virginia (Firm HQ)

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Clifton, VA 20124
Telephone: (202) 466-6937
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Arizona

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Bldg. 6, Ste 133
Gilbert, AZ 85295
Telephone: (602) 388-8899
Telecopier: (602) 393-4361