Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Drug Control Governance: Regulatory Bodies and Their Impact01:03

Drug Control Governance: Regulatory Bodies and Their Impact

Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with a...
Global Regulatory Systems01:28

Global Regulatory Systems

Global regulatory systems in bacteria enable rapid and coordinated responses to environmental changes by integrating sensory inputs with gene expression, ensuring efficient adaptation to fluctuating conditions. Key global regulatory mechanisms include regulons, two-component systems, sigma factors, and secondary messengers.Regulons and Global RegulatorsA regulon is a collection of genes and operons controlled by a common global regulator. These regulators enable bacteria to prioritize resource...
Drug Regulation01:25

Drug Regulation

Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
Standards of Care II01:19

Standards of Care II

Nurses bear specific legal responsibilities under several federal statutes, including:
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions01:15

Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions

PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Surgical lifestyles: going the distance in the OR and in athletics.

Bulletin of the American College of Surgeons·2013
Same author

Hospitals go green. Trustees discover that being gentle to the environment can actually save money.

Trustee : the journal for hospital governing boards·2011
Same author

Hospital-physician alignment.

Trustee : the journal for hospital governing boards·2011
Same author

Crunch time. CIOs balance cost and flexibility to plan for storing large volumes of diagnostic imaging data.

Healthcare informatics : the business magazine for information and communication systems·2010
Same author

Managing diversity, a look at where we are.

Health progress (Saint Louis, Mo.)·2010
Same author

Threat assessment. Enterprise risk management helps hospitals prepare for the unexpected.

Trustee : the journal for hospital governing boards·2010

Related Experiment Video

Updated: Jul 14, 2026

Working with Human Tissues for Translational Cancer Research
07:48

Working with Human Tissues for Translational Cancer Research

Published on: November 26, 2015

What boards need to know about regulatory issues.

Karen Sandrick

    Trustee : the Journal for Hospital Governing Boards
    |June 2, 2007
    PubMed
    Summary

    This series explains the Emergency Medical Treatment and Labor Act (EMTALA) for board members. It covers essential regulatory issues impacting healthcare governance and compliance.

    Area of Science:

    • Healthcare Regulation
    • Medical Governance
    • Compliance Management

    Background:

    • Understanding regulatory landscapes is crucial for healthcare boards.
    • The Emergency Medical Treatment and Labor Act (EMTALA) presents specific governance challenges.
    • A clear explanation of EMTALA is needed for effective board oversight.

    Purpose of the Study:

    • To provide a foundational understanding of EMTALA for board members.
    • To outline key regulatory considerations related to EMTALA.
    • To support informed decision-making in healthcare governance.

    Main Methods:

    • A review of EMTALA regulations and relevant legal interpretations.
    • Analysis of board responsibilities concerning patient access to care.

    More Related Videos

    Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes
    07:55

    Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes

    Published on: May 31, 2011

    Related Experiment Videos

    Last Updated: Jul 14, 2026

    Working with Human Tissues for Translational Cancer Research
    07:48

    Working with Human Tissues for Translational Cancer Research

    Published on: November 26, 2015

    Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes
    07:55

    Using SCOPE to Identify Potential Regulatory Motifs in Coregulated Genes

    Published on: May 31, 2011

  • Explanation of compliance requirements and potential liabilities.
  • Main Results:

    • Boards must be aware of EMTALA's requirements for emergency care.
    • Understanding EMTALA is vital for ensuring patient rights and hospital obligations.
    • Key regulatory aspects impacting board duties are detailed.

    Conclusions:

    • Comprehensive knowledge of EMTALA is essential for effective healthcare board governance.
    • Proactive compliance with EMTALA mitigates legal and operational risks.
    • This series serves as a critical resource for board members navigating healthcare regulations.