Global regulations corpus
Browse 15,074 regulations from 36 regulators
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Showing 151–200 of 256 regulations
Nonprescription Human Drug Products Subject to Section 760 of the Federal Food, Drug, and Cosmetic Act
21 CFR Part 329 establishes postmarketing adverse event reporting requirements for nonprescription human drugs under FD&C Act Section 760. Manufacturers must submit Individual Case Safety Reports (ICSRs) electronically to FDA containing patient information, adverse event details, suspect product data, reporter information, and responsible person contact details. Reports must include outcomes, dates, medical narratives, test results, product identifiers (NDC, lot number), dosing information, and concomitant medications. Patient names should be replaced with unique identification codes to protect privacy.
Investigational New Drug Application
This regulation establishes procedures and requirements for Investigational New Drug (IND) applications submitted to the FDA. It defines the scope of clinical investigations subject to IND requirements, specifies exemptions (including lawfully marketed drugs, in vitro diagnostics, laboratory research-only drugs, and certain placebo studies), and references institutional review and informed consent standards. The regulation governs which drug products must obtain FDA approval before conducting clinical trials.
Applications for FDA Approval to Market a New Drug
21 CFR Part 314 establishes procedures for submitting new drug applications (NDAs) and abbreviated new drug applications (ANDAs) to the FDA for approval to market new drugs under the Federal Food, Drug, and Cosmetic Act. The regulation outlines the agency's drug review process, defines key terms including active ingredients and exclusivity periods, and sets requirements for amendments, supplements, and postmarketing reports, while excluding designated medical gases and certain biologics subject to separate licensing provisions.
Section 804 Importation Program
Section 804 Importation Program establishes FDA procedures for time-limited programs permitting importation of eligible prescription drugs from Canada. The rule defines eligible drugs as FDA-approved medications available in the U.S. that also meet Canadian regulatory requirements, excluding controlled substances, biologics, and certain high-risk formulations like injectables and inhaled drugs. Importers must follow specified compliance, labeling, and adverse event reporting requirements.
Landfill and deposit for recovery: aftercare and permit surrender
Guidance on activities required during the aftercare phase of landfill and waste deposit facilities, and procedural requirements for applications to surrender environmental permits for such operations.
Fairer, faster redress in the energy market
We are seeking views on strengthening the role and powers of the Energy Ombudsman in the retail energy market.
Road fuel prices: 22 June 2026
UK government statistical announcement of weekly prices for unleaded petrol and diesel fuel, providing market pricing data for road fuel products.
Waste: export and import
UK guidance on regulatory controls governing the transport of waste into and out of England, including documentation, permitting, and compliance requirements for waste exporters and importers.
Public Sector Decarbonisation Scheme: delivery data
This publication provides delivery data for the Public Sector Decarbonisation Scheme (PSDS) phases 1 through 4, compiled from reports submitted to DESNZ (Department for Energy Security and Net Zero) via Salix Finance, tracking progress in decarbonising UK public sector facilities and operations.
Water and sewerage companies: EPA methodology for 2026 to 2030
This document outlines the methodology used by the Environment Agency and Natural Resources Wales to conduct annual Environmental Performance Assessments (EPA) of water and sewerage companies operating in England and Wales during the 2026-2030 period.
Sub-national estimates of properties not connected to the gas network 2015-2025
UK statistical release providing sub-national estimates of domestic properties not connected to the gas network, broken down by region and local authority, covering the period 2015-2025.
Sub-national gas consumption in Northern Ireland: 2015-2025
Statistical publication tracking gas consumption across Northern Ireland's local council areas from 2015 to 2025, providing sub-national energy consumption data.
Sub-national gas consumption at postcode level in 2025
UK statistical announcement for sub-national gas consumption data at postcode level in 2025, providing granular geographic breakdown of gas usage across the country.
Sub-national gas consumption at LSOA, MSOA and IGZ level in 2025
UK government announcement of sub-national gas consumption data for 2025, disaggregated at Lower Super Output Area (LSOA), Middle Super Output Area (MSOA), and Intermediate Geography Zone (IGZ) levels for statistical and energy monitoring purposes.
Sub-national gas consumption in 2025
UK statistical announcement for sub-national gas consumption data broken down by local authority in Great Britain for 2025. This reporting initiative tracks and publishes regional gas consumption patterns to support energy policy and planning at local levels.
Sub-national electricity consumption at postcode level in 2025
UK government statistical announcement regarding sub-national electricity consumption data at postcode level for 2025, providing granular geographic distribution of electricity usage across the country.
Sub-national electricity consumption at LSOA, MSOA and IGZ level in 2025
UK government statistics announcement for 2025 sub-national electricity consumption data disaggregated at Lower Super Output Area (LSOA), Middle Super Output Area (MSOA), and Intermediate Geography Zone (IGZ) levels.
Sub-national electricity consumption in 2025
UK statistical announcement detailing electricity consumption measurements disaggregated by local authority across Great Britain for 2025, supporting regional energy monitoring and policy development.
Great British Insulation Scheme release: June 2026
UK statistical release monitoring the installation of energy efficiency measures in domestic properties through the Great British Insulation Scheme (GBIS), scheduled for June 2026.
Road fuel prices: 15 June 2026
UK government publication announcing weekly price data for unleaded petrol and diesel fuel, released 15 June 2026.
The Environment Agency (NPS/WR/046060): application made to abstract water
The Environment Agency has submitted an application to the Secretary of State for Environment, Food and Rural Affairs requesting a licence to abstract water.
Producer responsibility regulations
UK producer responsibility regulations require producers to manage the end-of-life treatment and recycling of packaging, electrical and electronic equipment (EEE), batteries, and end-of-life vehicles (ELVs), establishing environmental and reporting obligations across these product categories.
Extended producer responsibility for packaging: who is affected and what to do
UK guidance for organisations that supply or import packaging on compliance with extended producer responsibility (EPR) requirements, including obligations to report on and manage packaging waste throughout its lifecycle.
UK government conversion factors for company reporting of greenhouse gas emissions
UK government conversion factors enable organisations to calculate and report greenhouse gas emissions from their UK operations using activity data such as fuel consumption and energy use.
Greenhouse gas reporting: conversion factors 2026
UK conversion factors for 2026 enable organisations to calculate and report greenhouse gas emissions from their UK activities, supporting compliance with mandatory emissions reporting requirements.
National Energy Efficiency Data-Framework (NEED): anonymised data 2026
The National Energy Efficiency Data-Framework (NEED) releases anonymised property-level data covering gas and electricity consumption from 2005 to 2024, alongside property characteristics and records of installed energy efficiency measures, supporting analysis of residential energy performance trends.
National Energy Efficiency Data-Framework (NEED)
The National Energy Efficiency Data-Framework (NEED) is a UK government collection of documents that consolidates information and guidance on energy efficiency data collection, analysis, and reporting. It serves as a central resource for energy efficiency regulatory and policy documentation.
National Energy Efficiency Data-Framework (NEED): consumption data tables 2026
Publication of National Energy Efficiency Data-Framework (NEED) consumption data tables for 2026, providing household energy consumption data for analysis and monitoring of energy efficiency trends in UK residential properties.
General Allocation and Price Rules
10 CFR Part 210 establishes recordkeeping requirements for firms subject to DOE allocation and price rules. Records must be maintained for transactions and expenses prior to specified dates, with ongoing obligations for firms involved in DOE litigation, those making restitutionary payments under orders, and firms undergoing audits. Record retention periods vary by firm category and may be extended or terminated by DOE notification.
Voluntary Greenhouse Gas Reporting Program: General Guidelines
This regulation establishes the Voluntary Reporting of Greenhouse Gases Program under the Energy Policy Act of 1992, setting procedures and requirements for entities to submit annual reports of greenhouse gas emissions, reductions, and sequestration activities. Reporting entities must file entity statements, use approved calculation methods, maintain records, and obtain certifications. Entities may report emissions back to 1990 and reductions back to 1991. Registration of reductions requires achievement after 2002 and compliance with entity-wide emission inventory quality standards, with different requirements for large and small emitters.
Renewable Energy Production Incentives
10 CFR Part 451 establishes Department of Energy incentive payment procedures for qualified renewable energy facilities owned by states, political subdivisions, not-for-profit cooperatives, public utilities, Indian tribes, or Native corporations. Eligible renewable sources include solar, wind, ocean, geothermal, and biomass energy. Payments are based on net electric energy generated and sold, with facility eligibility determined by date of first use and permit receipt.
Mandatory Petroleum Price Regulations
This regulation establishes mandatory reporting requirements for crude oil producers conducting enhanced oil recovery projects. Operators must file annual prepaid expenses reports with the Department of Energy by January 31 each year, documenting the nature, timing, and allocation of prepaid expenses for injectants, fuels, and other items used in tertiary recovery operations after September 30, 1981. Reporting continues until all prepaid expenses and their actual use are fully documented.
Collection of Information
10 CFR Part 207 establishes procedures for the Department of Energy to collect and enforce compliance with energy information reporting requirements under the Energy Supply and Environmental Coordination Act of 1974. It defines energy information broadly to include fuel reserves, exploration, production, distribution, consumption data, and related corporate and financial information. The regulation outlines violation procedures, notice requirements, and remedial order processes for entities failing to provide or circumventing energy information collection.
Epidemiology and Other Health Studies Financial Assistance Program
DOE regulation establishing grant and cooperative agreement procedures for epidemiological and health studies research, education, and communication activities. Covers health effects from DOE operations and energy production, including studies of worker and community health near DOE facilities, toxic substance exposure (including beryllium), and biomarker use for exposure recognition.
Standby Mandatory International Oil Allocation
This regulation implements U.S. obligations under the International Energy Program (IEP) to enable mandatory international oil allocation during energy supply emergencies. It applies to firms engaged in producing, transporting, refining, distributing or storing oil under U.S. jurisdiction. The rule remains on standby status and activates only when the President determines allocation is necessary to fulfill IEP obligations and notifies Congress; it reverts to standby within 60 days of emergency deactivation.
Certification, Compliance, and Enforcement for Consumer Products and Commercial and Industrial Equipment
10 CFR Part 429 establishes procedures for certification, compliance determination, and enforcement of energy conservation standards for consumer products and commercial/industrial equipment including HVAC systems, boilers, refrigeration equipment, and electric motors. Manufacturers must comply with applicable energy conservation standards from 10 CFR Parts 430 and 431, with certification conducted by independent, nationally recognized programs following ISO/IEC 17025 and NIST standards.
Fees for Facilities, Materials, Import and Export Licenses, and Other Regulatory Services Under the Atomic Energy Act of 1954, as Amended
10 CFR Part 170 establishes fees charged by the Nuclear Regulatory Commission for licensing services, inspection services, and special projects under the Atomic Energy Act of 1954. The regulation applies to applicants and holders of various nuclear licenses and approvals, including byproduct material licenses, source material licenses, special nuclear material licenses, power reactor operating licenses, spent fuel storage facilities, and import/export licenses, as well as fees for reactor operator examinations, inspections, and preapplication reviews.
International Voluntary Agreements
This regulation establishes standards and procedures for persons in the petroleum industry (producers, transporters, refiners, distributors, and storage operators) to develop voluntary agreements implementing the International Energy Program's information and allocation provisions during international energy supply emergencies, with meetings chaired by DOE and antitrust exemptions provided under the Energy Policy and Conservation Act.
Annual Fees for Reactor Licenses and Fuel Cycle Licenses and Materials Licenses, Including Holders of Certificates of Compliance, Registrations, and Quality Assurance Program Approvals and Government Agencies Licensed by the NRC
This regulation establishes annual fee requirements for persons holding nuclear reactor licenses, fuel cycle licenses, materials licenses, Certificates of Compliance, sealed source and device registrations, and quality assurance program approvals issued by the NRC. Fees apply to operating test reactors, research reactors, power reactors, and combined license holders after power ascension testing completion, as well as materials licensees and government agencies. The regulation defines key terms including budget authority and bundled units for small modular reactors, with bundled units up to 4,500 MWt assessed as single units.
Administrative Procedures with Respect to the Import and Export of Natural Gas
Establishes administrative procedures and rules for obtaining Department of Energy authorizations to import or export natural gas under the Natural Gas Act. Defines key terms including "natural gas," "contested proceedings," "interested persons," and procedural roles for decisional employees and the Assistant Secretary for Fossil Energy. Implements delegated authority from the DOE Act to regulate natural gas trade.
Collection of Foreign Oil Supply Agreement Information
This regulation requires persons with equity interests or contractual rights to extract crude oil from foreign countries to report detailed information about their supply agreements to the Department of Energy, including parties, production volumes, pricing terms, payment obligations, and contract terms. Reports must be submitted within 60 days of forms issuance, 14 days of agreement execution, or upon material changes, with joint operators able to designate a single participant to report on behalf of the operation.
Procedures for Acquisition of Petroleum for the Strategic Petroleum Reserve
This regulation establishes procedures for the Department of Energy to acquire petroleum products for the Strategic Petroleum Reserve, including purchase, exchange, and deferral mechanisms. It defines key terms such as backwardation, contango, deferral, and exchange, and outlines the roles of contracting officers and relevant DOE offices in managing SPR petroleum acquisitions under federal acquisition regulations.
Technical Regulation for Data Registration Procedures and the Issuance of Energy Efficienc...
Saudi Arabian technical regulation establishing data registration procedures and requirements for energy efficiency certification and issuance processes.
National Energy Efficiency Data-Framework (NEED) report: summary of analysis 2026
The National Energy Efficiency Data-Framework (NEED) report presents analysis of energy consumption trends from 2005 to 2024, providing a comprehensive summary of energy efficiency data in the UK using consumption patterns over a two-decade period.
Mammography
21 CFR Part 900 implements the Mammography Quality Standards Act (MQSA) by establishing procedures for FDA-approved accreditation bodies to evaluate mammography facilities and setting minimum national quality standards. The regulation defines key terms related to mammography operations, including accreditation bodies, adverse events (poor image quality, delayed reporting, unqualified personnel), air kerma measurement, and continuing education requirements for clinical staff.
Premarket Tobacco Product Applications
21 CFR Part 1114 establishes procedures and requirements for submitting premarket tobacco product applications (PMTAs) to the FDA, including evaluation procedures and postmarket reporting obligations. The regulation defines key terms such as tobacco product accessories, additives, adverse experiences, brand characteristics, and composition, and specifies the scope of applicability, excluding premium cigars and modified risk tobacco product applications unless they seek dual marketing orders.
General
21 CFR Part 1105 establishes FDA's premarket submission requirements for tobacco products. The regulation specifies grounds for refusing to accept applications, including submissions that lack required contact information, English translation, proper FDA forms, product identification details, environmental assessments, or a U.S. agent signature for foreign applicants. Accepted submissions receive a tracking number and processing acknowledgement.
Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
21 CFR Part 607 establishes establishment registration and product listing requirements for manufacturers of human blood and blood products, as well as manufacturers of licensed devices and biological products used in device manufacturing. The regulation defines key terms including blood products, establishments, manufacturing processes, and commercial distribution, and applies to blood banks, plasma donor centers, transfusion services, and independent testing laboratories.
Irradiation in the Production, Processing, and Handling of Animal Feed and Pet Food
21 CFR Part 579 establishes safety standards for using ionizing radiation in animal feed and pet food production. Facilities may use gamma rays (cobalt-60, cesium-137) or electrons (up to 10 MeV) to treat complete animal diets and ingredients. For poultry feed, additional X-ray sources are permitted. Minimum effective dose for salmonella control is 2.0 kGy; maximum is 25 kGy. Facilities must comply with Part 507 and incorporate applicable Part 179 food irradiation regulations.
Voluntary Filing of Cosmetic Product Ingredient Composition Statements
21 CFR Part 720 establishes a voluntary program for manufacturers, packers, and distributors of cosmetic products to file ingredient composition statements with the FDA on Form FDA 2512. Filings must occur within 180 days of the rule's effective date for existing products, or within 60 days of commercial distribution for new products. The filing requires disclosure of product name, manufacturer details, brand name, cosmetic category, and complete ingredient listings, with information made available to poison control centers and licensed physicians for safety and medical purposes.