Anesthetic and Analgesic Drug Products Advisory Committee

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Stored: Anesthetic and Analgesic Drug Products Advisory Committee

Anesthetic and Analgesic Drug Products Advisory Committee
Type: Boards, Commissions, and Committees
Parent organization: Food and Drug Administration
Top organization: Department of Health and Human Services
Employees:
Executive: Designated Federal Officer
Budget:
Address: 10903 New Hampshire Ave, Silver Spring, MD 20993
Website: https://www.fda.gov/advisory-committees/anesthetic-and-analgesic-drug-products-advisory-committee
Creation Legislation:
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Anesthetic and Analgesic Drug Products Advisory Committee
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Mission
Provide Food and Drug Administration (FDA) expert advice on anesthetic, analgesic drug safety, effectiveness, ensuring safe use, standards, pain management
Services

Review and evaluation of drug products; advisory consultations; safety assessments

Regulations

Clean Air Act; Clean Water Act; Comprehensive Environmental Response, Compensation, and Liability Act; Resource Conservation and Recovery Act; Safe Drinking Water Act (relevant to drug safety and environmental impact)

Anesthetic and Analgesic Drug Products Advisory Committee (AADPAC) is part of the U.S. Food and Drug Administration (FDA) and advises on matters related to anesthetics, analgesics, and related drug products. Based in Silver Spring, Maryland, the committee reviews data and provides recommendations on drug safety, efficacy, and labeling.

Official Site

Mission

The mission of AADPAC is to advise the FDA on the safety, effectiveness, and appropriate use of anesthetic and analgesic drugs. This includes reviewing new drug applications, discussing post-approval studies, and addressing public health concerns related to these medications, particularly in the context of pain management and anesthesia.[1]

Parent organization

AADPAC is part of the Food and Drug Administration (FDA), which falls under the Department of Health and Human Services. The FDA is responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs.

Legislation

While not established by a specific piece of legislation, AADPAC operates under the authority of the FDA, which is empowered by various acts like the Federal Food, Drug, and Cosmetic Act. Its activities are influenced by broader regulatory frameworks concerning drug regulation.

Partners

  • Pharmaceutical companies for data submission and discussion
  • Academic and research institutions for ongoing research collaboration
  • Other FDA advisory committees for cross-disciplinary advice

Number of employees

The committee does not have permanent employees but consists of voting members, including experts in anesthesiology, analgesics, epidemiology, and consumer representatives.

Organization structure

AADPAC's structure includes:

Leader

The committee's proceedings are managed by the Designated Federal Officer (DFO).

Divisions

  • No formal divisions; the committee operates as a single entity with members appointed based on expertise.

List of programs

  • Regular meetings to review specific drug applications or broader issues like opioid abuse
  • Subcommittees for preliminary evaluations (when necessary)

Last total enacted budget

Specific budget information for AADPAC is not publicly disclosed, as it is a part of the FDA's broader budgetary allocations.

Staff

Staffing for meetings includes the DFO and support from FDA staff; however, the committee itself is composed of external experts who serve in an advisory capacity.

Funding

Funding for AADPAC activities is part of the FDA's overall budget for advisory committee operations.

Services provided

AADPAC provides recommendations on drug approval, labeling, and post-marketing surveillance. It focuses on ensuring that anesthetic and analgesic drugs meet high standards of safety and effectiveness, particularly addressing issues like addiction, side effects, and drug interactions.[2]

Headquarters address

10903 New Hampshire Ave, Silver Spring, MD 20993

History

AADPAC was chartered to provide scientific and technical advice on drugs used in anesthesia and pain management. Its charter is regularly renewed, typically every two years, to continue its advisory role. The committee's history includes pivotal discussions on drug safety, particularly in the context of the opioid crisis and advancements in pain relief technologies.

External links

References

  1. Food and Drug Administration (2025). "Anesthetic and Analgesic Drug Products Advisory Committee". FDA.
  2. Food and Drug Administration (2025). "Human Drug Advisory Committees". FDA.