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Home Featured

Open Letter to DEA Administrator Milgram

Directly oversee the investigation of your DEA agents

Daily Remedy by Daily Remedy
May 15, 2023
in Featured
0
An Open Letter to DEA Administrator Milgram

DEA Washington, DC Division Office

Dear Administrator Anne Milgram,

 

I hope this letter finds you well.

I request you to oversee the investigation into the misconduct of DEA agents in my case. I initially filed a complaint with the Office of Inspector General which has been transferred to the Drug Enforcement Agency Office of Professional Responsibility.

The DEA has shown a lack of willingness and an inability to uphold it standards of conduct. Oversight agencies have consistently shown repeated incidents of misconduct by DEA agents, with only a few receiving much, if any, accountability.

I understand you are trying to reform the DEA and to enact much-needed reform. I thank you for listening to the public and for delaying the implementation of restrictive telehealth policies. Now I ask you to review the misconduct by DEA agents who targeted me in 2017 and manipulated evidence in my case that led to an indictment in 2018.

These agents solicited perjured statements from former employees who were forging prescriptions using my DEA license. They materially altered evidence in my case, including falsifying a police report and submitting an affidavit with false claims that were known to be untrue at the time of submission.

How they did this was quite clever. They would tamper with evidence and then obtain perjured statements to corroborate the tampering. Let me provide an example. Look at the police report I filed against the employee who was forging scripts under my name. You will see the report claims I reported her brother for threatening me, but somehow did not report her forgeries. How could I report one but not the other? Her brother threatened me because I planned to report her to the police.

This fraud was then complemented by perjured statements taken during the grand jury testimony. The same employee was asked by federal prosecutors whether she had forged scripts under my name – to which that employee answered no with no pushback from either DEA agents or federal prosecutors. This is all the more curious, since both DEA agents and federal prosecutors had many forged prescriptions in their hand.

The misconduct is easy to discern when you parse through the evidence in this way. But it makes the efforts to distort evidence in this case all the more concerning. And it’s precisely why you must directly intervene in this investigation.

I have written a book that details the misconduct by the DEA in this case. I also compiled all legal documents in this case and plan to share them with investigative journalists and criminal justice reform organizations. These efforts are intended to raise awareness of the misconduct in my case. I plan to involve all interested parties in the review of DEA misconduct. Thank you in advance for your time and effort.

 

Respectfully,

Dr. Jay K Joshi

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Daily Remedy

Daily Remedy

Dr. Jay K Joshi serves as the editor-in-chief of Daily Remedy. He is a serial entrepreneur and sought after thought-leader for matters related to healthcare innovation and medical jurisprudence. He has published articles on a variety of healthcare topics in both peer-reviewed journals and trade publications. His legal writings include amicus curiae briefs prepared for prominent federal healthcare cases.

Comments 0

  1. Jrae says:
    3 years ago

    I commend you for challenging the DEA. We cannot leave this Agency unaccountable they have destroyed many lives.

    Reply

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Videos

summary

An in-depth exploration of drug pricing, including key databases like NADAC, WAC, and ASP, and how they influence the pharmaceutical supply chain, policy, and patient advocacy. The episode also introduces MedPricer's innovative pricing intelligence platform, offering valuable insights for healthcare professionals, policymakers, and patients.

Chapters

00:00 Understanding Drug Pricing Dynamics
03:52 Exploring the Drug Pricing Database
10:07 Patient Advocacy and Drug Pricing
13:56 Market Intelligence in Drug Pricing
How NADAC, WAC, and ASP Shape Drug CostsDaily Remedy
YouTube Video X-Tfwy7XKEg
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Policy Shift in Peptide Regulation

Clinical Reads

FDA Evaluation of Certain Bulk Drug Substances in Compounding: Clinical Interpretation

FDA Evaluation of Certain Bulk Drug Substances in Compounding: Clinical Interpretation

by Daily Remedy
April 19, 2026
0

Clinicians increasingly encounter patients using or requesting peptide-based therapies sourced through compounding pharmacies. The U.S. Food and Drug Administration has identified a subset of bulk drug substances, including certain peptides, that may present significant safety risks when used in compounded formulations. The clinical question is whether these regulatory signals reflect meaningful patient-level risk and how they should influence prescribing behavior. This matters because compounded peptides often sit outside traditional approval pathways, creating uncertainty around quality, dosing consistency, and safety. Understanding...

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