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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.
Bioavailability and Bioequivalence Requirements
21 CFR Part 320 establishes FDA requirements for demonstrating bioavailability and bioequivalence of drug products in new drug applications, abbreviated new drug applications, and supplemental applications. Applicants must submit evidence of in vivo bioavailability for full NDAs or demonstrate bioequivalence to a reference listed drug for abbreviated NDAs, with FDA authority to waive certain requirements or require additional study reports when concerns arise.
Certification and Postmarketing Reporting for Designated Medical Gases
21 CFR Part 230 establishes FDA procedures for certification and postmarketing surveillance of designated medical gases. It requires applicants to submit certifications under the Federal Food, Drug, and Cosmetic Act and defines requirements for adverse event reporting, including serious adverse events. The regulation sets minimum data standards for individual case safety reports and establishes postmarketing safety monitoring systems.
Drugs; Official Names and Established Names
21 CFR Part 299 establishes procedures for designating official and established names for drugs under the Federal Food, Drug, and Cosmetic Act. The regulation defines official names as those designated by the FDA Commissioner under section 508, and established names as official names, compendial names, or common/usual names. The FDA recognizes the U.S. Adopted Names Council for deriving nonproprietary drug names and generally relies on compendial or common names rather than routinely designating new official names.
General
This regulation establishes FDA policies for fixed-combination prescription drugs, prohibits chlorofluorocarbon propellants in human drugs, and requires annual reporting by manufacturers and sponsors of eligible investigational drugs supplied to eligible patients under the Right to Try Act.
Controlled Drugs
21 CFR Part 290 establishes requirements for dispensing controlled substances scheduled II–V under the Federal Controlled Substances Act. Drugs in these schedules require prescription-only dispensing unless exempted (e.g., codeine preparations ≤200 mg per 100 mL/g with non-narcotic active ingredients). Labels must carry a federal warning prohibiting unauthorized transfer. Emergency oral prescriptions of Schedule II drugs are permitted when immediate administration is medically necessary and written prescription is impractical.
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.
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.
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): 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Clinical Chemistry and Clinical Toxicology Devices
21 CFR Part 862 establishes the FDA classification framework for clinical chemistry and clinical toxicology devices intended for human use. It defines the scope of device regulation, specifies that calibrators used with these devices are classified as Class II regardless of the device's classification due to their critical role in measurement accuracy, and outlines the premarket approval requirements and effective dates for devices classified as Class III.
Miscellaneous
21 CFR Part 1307 establishes miscellaneous provisions for controlled substance regulation under DEA authority. It clarifies that state and federal law requirements remain in effect, allows practitioners to request regulatory exceptions, permits registered dispensers to distribute controlled substances to other practitioners up to 5% of their annual dispensed volume without separate distributor registration, and exempts incidental controlled substance manufacturing by registered manufacturers from additional registration requirements.
Food Additive Petitions
21 CFR Part 571 establishes the procedure for submitting food additive petitions to the FDA under the Federal Food, Drug, and Cosmetic Act. Petitioners must submit applications in triplicate with detailed information on the food additive's chemical identity, composition, manufacturing methods, analytical controls, stability data, and proposed uses. The regulation specifies content requirements including physical/chemical/biological properties, specifications, impurities, and manufacturing details for each entity involved in production.
Hematology and Pathology Devices
21 CFR Part 864 establishes the regulatory framework for hematology and pathology devices intended for human use in commercial distribution. It outlines classification requirements, premarket approval timelines for Class III devices, and exemptions from premarket notification under section 510(k) of the Federal Food, Drug, and Cosmetic Act. Manufacturers must demonstrate substantial equivalence to existing devices and comply with applicable FDA guidance.
Quotas
This regulation establishes procedures for DEA quotas on Schedule I and II controlled substances. It defines three quota types—aggregate production, individual manufacturing, and procurement—and five subcategories covering commercial sale, transfers, product development, and replacement of disposed material. Quotas limit the total and per-manufacturer quantities of controlled substance APIs that may be produced or procured annually for pharmaceutical manufacturing.