Interest Archives - Page 46 of 57 - Food and Drug Law Institute (FDLI)

Getting by with a Little Help from Their Friends: FDA Using External Experts to Enhance Biomarker Qualification and Enable Precision
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Getting by with a Little Help from Their Friends: FDA Using External Experts to Enhance Biomarker Qualification and Enable Precision

Archived Publication, Drugs, Medical Devices, Biologics, Food and Drug Law Journal, Publications, Volume 72.4

Getting by with a Little Help from Their Friends: FDA Using External Experts to Enhance Biomarker Qualification and Enable Precision

Food and Drug Law Journal | Volume 72 | Number 4

Getting by with a Little Help from Their Friends: FDA Using External Experts to Enhance Biomarker Qualification and Enable Precisionadmin2021-04-21T16:16:01-04:00

Letter to the Editor
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Letter to the Editor

Archived Publication, Food and Drug Law Journal, Food, Dietary Supplements, Cosmetics, Publications, Volume 72.4

Letter to the Editor

Food and Drug Law Journal | Volume 72 | Number 4

Letter to the Editoradmin2021-04-21T16:19:21-04:00

Editorial or Ad? FTC’s Native Advertising Guidelines and Challenges for Industry
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Editorial or Ad? FTC’s Native Advertising Guidelines and Challenges for Industry

Drugs, Medical Devices, Biologics, Event, Food, Dietary Supplements, Cosmetics, General Webinars, On-demand Webinar, Tobacco Products

Editorial or Ad? FTC’s Native Advertising Guidelines and Challenges for Industry

Recorded November 29, 2017 | On-Demand Webinar

Editorial or Ad? FTC’s Native Advertising Guidelines and Challenges for Industryadmin2024-07-19T09:46:49-04:00

Development of Medical Devices: Best Practices for Safeguarding Your IP and FDA Rights
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Development of Medical Devices: Best Practices for Safeguarding Your IP and FDA Rights

Drugs, Medical Devices, Biologics, Event, Medical Products Webinars, On-demand Webinar

Development of Medical Devices: Best Practices for Safeguarding Your IP and FDA Rights

Recorded November 17, 2017 | On-Demand Webinar

Development of Medical Devices: Best Practices for Safeguarding Your IP and FDA Rightsadmin2024-07-19T09:45:24-04:00

Drug Quality Security Act Conference
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Drug Quality Security Act Conference

Archived Event, Drugs, Medical Devices, Biologics, Event

Drug Quality Security Act Conference

November 15, 2017 I Washington, DC

Drug Quality Security Act Conferenceadmin2018-12-07T10:56:55-05:00

FDA, USDA, and EPA: Inter-Agency Overlap and Jurisdictional Boundaries
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FDA, USDA, and EPA: Inter-Agency Overlap and Jurisdictional Boundaries

Event, Food and Dietary Supplements Webinars, Food, Dietary Supplements, Cosmetics, On-demand Webinar

FDA, USDA, and EPA: Inter-Agency Overlap and Jurisdictional Boundaries

Recorded November 9, 2017 | On-Demand Webinar

FDA, USDA, and EPA: Inter-Agency Overlap and Jurisdictional Boundariesadmin2020-05-19T15:15:05-04:00

Compounding the Off-Label Promotion Debate: How FDA Could Regulate the Promotion of Unapproved Drugs
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Compounding the Off-Label Promotion Debate: How FDA Could Regulate the Promotion of Unapproved Drugs

Archived Publication, Drugs, Medical Devices, Biologics, Publications, Update Magazine, Update September/October 2017

Compounding the Off-Label Promotion Debate: How FDA Could Regulate the Promotion of Unapproved Drugs

Update Magazine | September/October 2017

Compounding the Off-Label Promotion Debate: How FDA Could Regulate the Promotion of Unapproved Drugsadmin2017-11-16T13:49:29-05:00

Intellectual Property for the Food and Drug Law Professional: Issues that Arise in the Product Development Process
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Intellectual Property for the Food and Drug Law Professional: Issues that Arise in the Product Development Process

Archived Publication, Drugs, Medical Devices, Biologics, Publications, Update Magazine, Update September/October 2017

Intellectual Property for the Food and Drug Law Professional: Issues that Arise in the Product Development Process

Update Magazine | September/October 2017

Intellectual Property for the Food and Drug Law Professional: Issues that Arise in the Product Development Processadmin2017-11-16T13:49:39-05:00

The “New” NDC: Are You Aware of FDA’s Rollout of the New Unique Medical Device Identifier (UDI) and Its Potential Future Impact on Payer Claims Forms?
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The “New” NDC: Are You Aware of FDA’s Rollout of the New Unique Medical Device Identifier (UDI) and Its Potential Future Impact on Payer Claims Forms?

Archived Publication, Drugs, Medical Devices, Biologics, Publications, Update Magazine, Update September/October 2017

The “New” NDC: Are You Aware of FDA’s Rollout of the New Unique Medical Device Identifier (UDI) and Its Potential Future Impact on Payer Claims Forms?

Update Magazine | September/October 2017

The “New” NDC: Are You Aware of FDA’s Rollout of the New Unique Medical Device Identifier (UDI) and Its Potential Future Impact on Payer Claims Forms?admin2017-11-16T13:49:48-05:00

FDA’s Comprehensive Approach to Nicotine and Tobacco
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FDA’s Comprehensive Approach to Nicotine and Tobacco

Archived Publication, Publications, Tobacco Products, Update Magazine, Update September/October 2017

FDA’s Comprehensive Approach to Nicotine and Tobacco

Update Magazine | September/October 2017

FDA’s Comprehensive Approach to Nicotine and Tobaccoadmin2017-11-16T13:53:25-05:00