Information and Regulatory Affairs | OMB | The White House (2024)

FAQs

What is the goal of the Office of Information and Regulatory Affairs (OIRA)? ›

In addition to reviewing collections of information under the Paperwork Reduction Act, OIRA reviews draft regulations under Executive Order 12866 and develops and oversees the implementation of government-wide policies in the areas of information technology, information policy, privacy, and statistical policy.

For all significant regulatory actions, the Executive Order requires OIRA review before the actions take effect. Under EO 12866, OIRA has up to 90 days (which can be extended) to review a rule.

OIRA is part of the Office of Management and Budget (OMB), which is an agency within the Executive Office of the President.

OMB coordinates the development of the President's budget proposal by issuing circulars, memoranda, and guidance documents to the heads of executive agencies. Executive agencies may then prepare their budget requests in accordance with the instructions and guidance provided by OMB.

“Major rules” (ones that are economically significant and require OIRA review) must be made effective at least 60 days after the date of publication in the Federal Register, allowing time for Congressional review. In emergency situations, a major rule can be made effective before 60 days.

OIRA's review of draft significant rules or other regulatory actions is called “E.O. 12866 review,” after the Executive Order, and meetings with OIRA about actions that we are reviewing are called “E.O.

A regulation is a bit more formal than a rule – it prescribes the required conduct or action exactly; Rules are also binding, but, by contrast, describe what is generally considered to be the proper course of conduct. Codes are books where statutes (laws) or regulations on similar subjects are grouped together.

The Paperwork Reduction Act (PRA) requires Federal Agencies to submit proposed. collections of information for review and approval by the Office of Management and Budget.

Location: Washington, D.C. The Office of Information and Regulatory Affairs (OIRA) is a United States federal government office located within the Office of Management and Budget (OMB), itself a division of the Executive Office of the President.

Does the official IRA still exist? ›

The IRA – the Irish Republican Army - is a title most people associate with the Provisional IRA. But in fact, the Provisionals had broken away from what became known as the Official IRA at the beginning of the Troubles. The Officials went on ceasefire in 1972 – but never fully disappeared.

Once the OMB review is complete, the Desk Officer will notify the appropriate FRLO that the rulemaking has been approved for publication in the Federal Register. The FRLO will notify the action officer of OMB clearance and request the action officer forward the rule package to their PSA for approval.

OMB ensures that agency reports, rules, testimony, and proposed legislation are consistent with the president's budget and administration policies. OMB also oversees and coordinates the administration's procurement, financial management, information, and regulatory policies.

The White House Office is headed by the White House chief of staff, who is also the head of the Executive Office of the President. The staff work for and report directly to the president, including West Wing staff and the president's senior advisers.

1 Overview of Twenty-Fifth Amendment, Presidential Vacancy. Section 1: In case of the removal of the President from office or of his death or resignation, the Vice President shall become President.

Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines, and by the companies ...

The purpose of regulatory agencies is to protect the public's health, safety, property, and overall interests. In most cases, this involves setting, enforcing, and publicizing licensing requirements, quality standards, and conduct rules across an industry.

The Regulatory Affairs Officer ensures the appropriate licensing, marketing and legal compliance of medicinal products for human and veterinary use and of non-medicinal products (cosmetics, food supplements, medical devices, animal feed, …)

ORA is the lead office for all agency field activities. ORA inspects regulated products and manufacturers, conducts sample analyses of regulated products and reviews imported products offered for entry into the United States.