Compliance Frameworks
Regulatory Frameworks
Track regulatory news by compliance framework. From REACH to GDPR, stay ahead of the rules that matter.
REACH
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CLP
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RoHS
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TSCA
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CSRD
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EU Taxonomy
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ESRS
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MDR
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FDA 21 CFR
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ICH Guidelines
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AI Act
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EU GMP
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CS3D
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EUDR
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GHS
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Eudralex
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GVP
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FDA 510(k)
REACH
Registration, Evaluation, Authorisation and Restriction of Chemicals
EU regulation requiring companies to register and evaluate chemical substances to ensure safe use. REACH impacts manufacturers, importers, and downstream users across all industries dealing with chemical substances.
CLP
Classification, Labelling and Packaging Regulation
EU regulation aligning the classification, labelling, and packaging of chemical substances and mixtures with the UN Globally Harmonized System (GHS).
RoHS
Restriction of Hazardous Substances Directive
EU directive restricting the use of specific hazardous materials found in electrical and electronic products to protect human health and the environment.
TSCA
Toxic Substances Control Act
US federal law giving the EPA authority to regulate the introduction of new or already existing chemicals, including reporting, record-keeping, and testing requirements.
CSRD
Corporate Sustainability Reporting Directive
EU directive requiring large companies and listed SMEs to report on sustainability matters using European Sustainability Reporting Standards (ESRS).
EU Taxonomy
EU Taxonomy Regulation
EU classification system establishing criteria for environmentally sustainable economic activities to guide investment toward the EU's climate and environmental objectives.
ESRS
European Sustainability Reporting Standards
Standards developed by EFRAG defining the reporting requirements under CSRD, covering environmental, social, and governance topics.
MDR
Medical Device Regulation
EU regulation governing the production, distribution, and post-market surveillance of medical devices, replacing the previous Medical Device Directive.
FDA 21 CFR
FDA Title 21 Code of Federal Regulations
US regulations governing food, drugs, medical devices, biologics, and other products overseen by the FDA, covering manufacturing, labeling, and approval processes.
ICH Guidelines
International Council for Harmonisation Guidelines
Global guidelines harmonizing pharmaceutical development and registration requirements across regulatory authorities to ensure safe, effective, and high-quality medicines.
AI Act
EU Artificial Intelligence Act
EU regulation establishing a comprehensive legal framework for AI systems based on risk levels, from unacceptable to minimal risk, with specific obligations for high-risk AI.
EU GMP
EU Good Manufacturing Practice
European guidelines ensuring pharmaceutical products are consistently produced and controlled according to quality standards appropriate for their intended use.
CS3D
Corporate Sustainability Due Diligence Directive
EU directive requiring large companies to identify, prevent, and mitigate adverse human rights and environmental impacts in their operations and value chains.
EUDR
EU Deforestation Regulation
EU regulation requiring companies to ensure that products sold in the EU market have not contributed to deforestation or forest degradation.
GHS
Globally Harmonized System of Classification and Labelling
International standard for the classification of chemicals and the communication of hazard information through labels and safety data sheets.
Eudralex
Eudralex - EU Pharmaceutical Legislation
Collection of EU rules and regulations governing medicinal products, covering authorization, manufacturing, distribution, and pharmacovigilance.
GVP
Good Pharmacovigilance Practices
EU guidelines for the monitoring of the safety of medicinal products and the detection, assessment, and prevention of adverse effects.
FDA 510(k)
FDA 510(k) Premarket Notification
US regulatory pathway for demonstrating that a medical device is substantially equivalent to a legally marketed predicate device, required before market introduction.
Monitoring 200+ official sources worldwide
