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November 15, 2019

Laboratory Operations Manual

This document is an internal Drug Enforcement Administration quality system document.  The document is updated periodically and current as of November 15, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

October 28, 2019

Fentanyl Signature Profiling Program Report

The Fentanyl Signature Profiling Program (FSPP) performs in-depth chemical analyses on fentanyl and fentanyl-related exhibits obtained from seizures made throughout the United States.  This report details the results and conclusions derived from these analyses that are reported on a quarterly basis. FSPP data is not intended to reflect U.S. market share, but is rather a snapshot of samples submitted to this laboratory from the 7 DEA regional laboratories.

October 23, 2019

Analysis of Drugs Manual

This document is an internal Drug Enforcement Administration quality system document.  The document is updated periodically and current as of October 23, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL8 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Southwest Laboratory (SFL8).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL7 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Western Laboratory (SFL7).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL6 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the South Central Laboratory (SFL6).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL5 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the North Central Laboratory (SFL5).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL4 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Southeast Laboratory (SFL4).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL3 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Mid-Atlantic Laboratory (SFL3).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

April 25, 2019

SFL2 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Northeast Laboratory (SFL2).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

 

April 25, 2019

SFL1 Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated qualitative and quantitative methods from the Special Testing and Research Laboratory (SFL1).  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

 

April 25, 2019

Summary of Validated Methods

This document is an internal Drug Enforcement Administration quality system document which provides a summary of validated quantitative methods.  The document is updated periodically and current as of April 25, 2019 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

August 13, 2018

Latent Print Examination Manual

This document is an internal Drug Enforcement Administration quality system document for latent print examination.  The document is updated periodically and current as of August 13, 2018 and is provided for informational purposes only. Any sensitive, privileged or otherwise protected information has been redacted, to include the redaction of some documents in their entirety. All redactions are clearly present in this document. Names of commercial manufacturers are provided for identification only, and inclusion does not imply endorsement by the Drug Enforcement Administration.

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