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NAD Recommends that Medical Device Manufacturer Discontinue Advertising Claims Following Competitor Challenge
[07/11/24]
Preparing for Change: After 20 Years, HHS Proposes Update to Research Misconduct Regulations
[02/16/24]
A Whole New World for Laboratory Developed Tests – FDA Proposes End to Its Longstanding Policy of Enforcement Discretion
[11/30/23]
FDA Finalizes Its Informed Consent Guidance for IRBs, Clinical Investigators and Sponsors
[10/05/23]
FDA Outlines Considerations for Conducting Clinical Investigations Using Psychedelic Drugs
[09/15/23]
Embracing Technology: FDA Releases Draft Guidance on Decentralized Clinical Trials
[09/14/23]
U.S. Food and Drug Administration Issues Draft Guidance Updating Good Clinical Practices
[06/29/23]
Single Institutional Review Board Exception Determination Set to Expire May 11, 2023
[03/01/23]
Important Information for COVID-19 Vaccine Providers
[12/15/20]
Substance Use Disorder Providers Should Note SAMHSA Proposed Changes to 42 CFR Part 2
[08/30/19]
The Practice of Medicine vs. Protecting Patient Safety: Groundbreaking Court Ruling in Support of the FDA’s Regulation of Certain Stem Cell Therapies
[06/11/19]
Delay of “2018 Requirements” that Revise the Common Rule
[04/04/18]
New Guidance: FDA Allows Waiver of Informed Consent for Minimal Risk Research
[08/22/17]
CMS Proposes Significant Changes to the CJR Model and the Cancellation of the AMI, CABG and SHFFT Episode Payment Models
[08/16/17]
OIG Approves Waiver of Cost-Sharing Amounts for Financially Needy Beneficiaries Participating in Clinical Research Studies
[07/18/17]
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