Global regulations corpus
Browse 16,737 regulations from 36 regulators
2,890 updated in the last 30 days. Public corpus — no signup required to read.
Showing 1–50 of 54 regulations
Human Performance, Version 2
Personnel Certification: Radiation Safety Officers
Accident Management, Version 2
Maintenance Programs for Nuclear Power Plants
Safety Analysis for Class IB Nuclear Facilities
Fitness for Duty: Managing Worker Fatigue
Design of Uranium Mines and Mills: Ventilation Systems, Version 1.1
General Design Considerations: Human Factors
Nuclear Fuel Safety
Minimum Staff Complement
Conduct of Licensed Activities: Construction and Commissioning Programs
Management System
Design, Testing and Performance of Exposure Devices, Version 1.1
Reliability Programs for Nuclear Power Plants
Design of Rooms Where Unsealed Nuclear Substances Are Used
Deterministic Safety Analysis
Probabilistic Safety Assessment (PSA) for Reactor Facilities, Version 2
Safety Culture
Chemistry Control for Reactor Facilities
Periodic Safety Reviews
Operations Programs for Reactor Facilities
Personnel Training, Version 2
Design of Industrial Radiography Installations
Nuclear Criticality Safety, Version 1.1
Design of Reactor Facilities, Version 2.1
Aging Management
License to Operate a Launch Site
FAA regulation 14 CFR Part 420 establishes licensing requirements for persons operating commercial launch sites in the United States. The rule prescribes application procedures, safety demonstrations, approval bases, license terms, and post-licensing compliance obligations. Applicants must meet equivalent safety standards, with exemptions for amateur rocket operations. The regulation defines key technical terms including debris dispersion, casualty areas, and coordinate systems used in launch safety analysis.
Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food
21 CFR Part 117 establishes current good manufacturing practice (CGMP), hazard analysis, and risk-based preventive controls requirements for human food manufacturing, processing, packing, and holding facilities in the US. The regulation defines applicability, key food safety terms (including critical control points, allergen cross-contact, environmental pathogens), and compliance obligations under the Federal Food, Drug, and Cosmetic Act to prevent adulteration and contamination.
Thermally Processed Low-Acid Foods Packaged in Hermetically Sealed Containers
21 CFR Part 113 establishes regulatory requirements for thermally processed low-acid foods packaged in hermetically sealed containers. The regulation defines key concepts including commercial sterility, aseptic processing, critical factors, and equipment specifications to ensure microorganisms capable of reproducing under normal storage conditions are eliminated, protecting public health and maintaining product safety in shelf-stable food manufacturing.
Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food
21 CFR Part 110 establishes current good manufacturing practice (CGMP) standards for manufacturing, packing, and holding human food. The regulation defines key terms including acid foods, critical control points, food-contact surfaces, microorganisms, pests, sanitization, and quality control operations. It sets mandatory requirements (indicated by "shall") and advisory procedures to prevent food adulteration and ensure food safety through proper manufacturing and sanitation practices.
Processing and Bottling of Bottled Drinking Water
21 CFR Part 129 establishes current good manufacturing practice requirements for processing and bottling of bottled drinking water. The regulation mandates that facilities use approved water sources, maintain sanitary conditions throughout processing, bottling, holding, and shipping, and implement controls ensuring product safety. Key requirements include plant construction standards with separated bottling rooms, proper ventilation, enclosed container washing areas, and use of nontoxic materials for water-contact surfaces.
Yorkshire companies to pay hundreds of thousands after incidents
Following investigations by the Environment Agency, four Yorkshire companies will pay almost £470,000 after they breached environmental permits.
Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Food for Animals
This regulation establishes current good manufacturing practice (CGMP), hazard analysis, and risk-based preventive controls for animal food facilities in the US. It defines applicability criteria, prohibits operation of non-compliant animal food manufacturing facilities, and establishes requirements for hazard analysis and preventive controls. Facilities manufacturing both human and animal food may comply with human food standards instead if requirements are met.
Current Good Manufacturing Practice for Finished Pharmaceuticals
21 CFR Part 211 establishes minimum current good manufacturing practice (cGMP) standards for finished pharmaceutical drug products for human and animal use. The regulation requires establishment of a quality control unit with authority to approve/reject components, containers, in-process materials, and finished products; mandates adequate laboratory facilities for testing; and requires personnel to have appropriate education, training, and experience in manufacturing operations and cGMP requirements.
Current Good Manufacturing Practice for Medicated Feeds
21 CFR Part 225 establishes current good manufacturing practice (CGMP) standards for medicated feeds to ensure drug safety, identity, strength, quality, and purity. The regulation applies to all facilities and equipment used in medicated feed production, requires qualified personnel with adequate training and supervision, and mandates proper building construction, maintenance, and sanitation to prevent contamination and pest infestation.
Current Good Manufacturing Practice for Type a Medicated Articles
21 CFR Part 226 establishes current good manufacturing practice (CGMP) requirements for Type A medicated articles used in animal feeds. The regulation mandates that manufacturers maintain adequate personnel qualifications, facility construction and maintenance standards, and equipment controls to ensure products meet safety, identity, strength, quality, and purity specifications. Requirements include proper building design with adequate space for segregated operations, appropriate environmental controls, and facility maintenance protocols to prevent contamination and cross-mixing of products.
Human Drug Compounding
This regulation establishes FDA rules for human drug compounding under 21 CFR Part 216. It lists bulk drug substances approved for compounding (including Brilliant Blue G and several topical agents), identifies substances excluded from compounding (Oxitriptan, Piracetam, Silver Protein Mild, Tranilast), and sets FDA evaluation criteria based on physical/chemical characterization, safety, efficacy evidence, and historical use. Compounders cannot claim FDA approval for products made with listed substances.
Technical Regulation for Pressure Equipment
Saudi Arabian technical regulation establishing design, manufacturing, and safety requirements for pressure equipment. Sets standards for equipment that operates above specified pressure thresholds to ensure mechanical integrity, prevent failures, and protect workers and the public from hazards associated with pressurized systems.
Technical Regulation for Machinery Safety – Part 4: Cutting and Sawing Machines
Technical regulation establishing safety standards for cutting and sawing machines in Saudi Arabia. Covers design, construction, and operational requirements to protect workers from hazards associated with these machines, including guard systems, emergency stops, and safe operational procedures.
Technical Regulation for simple pressure vessels
Saudi technical regulation establishing standards for simple pressure vessels, covering design, manufacturing, testing, and safety requirements to ensure equipment reliability and worker protection in industrial applications.
Technical Regulation for Machinery Safety – Part 3: Lifting Equipment
Technical regulation establishing safety requirements for lifting equipment in Saudi Arabia. Covers design, manufacture, installation, operation and maintenance standards to protect workers and prevent accidents during material handling and lifting operations.
Technical Regulation for equipment safety: part 2
Saudi Arabian technical regulation establishing safety requirements for equipment. The regulation sets forth mandatory standards and compliance criteria to ensure equipment used in industrial and commercial applications meets prescribed safety benchmarks to protect workers and prevent hazards.
General Biological Products Standards
21 CFR Part 610 establishes general standards for licensed biological products in the US, requiring manufacturers to complete conformity tests on each product lot before release and permitting FDA oversight of lot samples and protocols. The regulation specifies testing requirements for potency, sterility, and safety, allows equivalent methods with FDA approval, and governs release procedures through the Center for Biologics Evaluation and Research or Center for Drug Evaluation and Research.
Medical Device Reporting
21 CFR Part 803 establishes medical device reporting requirements for device user facilities, manufacturers, importers, and distributors. Device user facilities must report deaths and serious injuries caused or contributed to by devices, maintain adverse event files, and submit annual summaries. Manufacturers and importers must report similar events and device malfunctions, while distributors must maintain incident records without reporting obligations. These requirements protect public health by ensuring devices remain safe, effective, and not adulterated or misbranded.
Performance Standards for Microwave and Radio Frequency Emitting Products
This regulation establishes performance standards for microwave ovens manufactured after October 6, 1971, setting limits on microwave radiation emission and requiring safety interlocks. Microwave ovens must not exceed 1 milliwatt per square centimeter power density at 5+ centimeters from the external surface before purchase, and 5 milliwatts per square centimeter thereafter. Devices must have at least two operative safety interlocks designed to prevent microwave generation when cavity access is possible, with at least one interlock resistant to human body contact and magnetic manipulation.
Controls to Satisfy the Requirements of the Act Applicable to the Manufacturing of Marihuana
21 CFR Part 1318 establishes regulatory controls for the registration and manufacturing of marihuana, including cultivation, growth, and harvest procedures. Registered manufacturers must deliver their total cannabis crops to the Administration within four months of harvest, with the Administration taking physical possession and controlling access. Applicants must demonstrate compliance with statutory requirements and public interest considerations under the Controlled Substances Act and international Single Convention obligations.
Technical Regulations for Tanks — Part 3: Dry Gas Transport Tanks
Saudi Arabian mandatory technical regulations establishing construction, pressure rating, safety device, marking, and inspection specifications for tanks used in road transport of dry gases.
Technical Regulation — Equipment and Protective Systems Intended for Use in Potentially Explosive Atmospheres
Saudi Arabian technical regulation mandating design, certification, and labeling requirements for equipment and protective systems used in potentially explosive atmospheres. Applies to oil & gas, refinery, and petrochemical operations operating in classified hazardous zones. Establishes conformity assessment and compliance marking procedures.
Technical Regulation — Requirements for Machinery Safety
Saudi Arabian technical regulation establishing essential health and safety requirements for industrial machinery placed on the market, aligned with EU Machinery Directive 2006/42/EC standards for machinery design, construction, and risk management.
Directive 2022/2557 on the resilience of critical entities
The CER Directive (2022/2557), effective 16 January 2023, requires EU Member States to identify critical entities by 17 July 2026 providing essential services across eleven sectors, including energy subsectors (electricity, aggregation, demand response, energy storage, district heating/cooling, oil, gas, hydrogen). These entities must enhance resilience against cyberattacks, natural disasters, and other threats to protect public health, safety, and the economy.