Jurisdiction
International
20 compliance framework entries tagged under this jurisdiction. Open each card for official documentation links.
- 20 frameworks
AS9100
OfficialAS9100D Quality Management Systems: Requirements for Aviation, Space, and Defense Organizations
AS9100D is the aviation, space and defense quality management system standard, published by SAE International and built on ISO 9001:2015.
CAP Accreditation
OfficialCAP Laboratory Accreditation Program
College of American Pathologists accreditation programs for laboratories, including the Laboratory Accreditation Program and CAP 15189.
Sustainability Reporting
OfficialESG and Sustainability Reporting Standards
Index of sustainability disclosure standards and rules, including GRI, ISSB (IFRS S1 and S2), SASB, the EU CSRD and SEC climate rules.
GCP
OfficialGood Clinical Practice (ICH E6(R3))
International standard for the design, conduct and reporting of clinical trials (ICH E6(R3)), issued by FDA as final guidance in the US.
ICH E6(R3) GCP
OfficialICH E6(R3) Good Clinical Practice
ICH's international guideline for the ethical and scientific conduct of clinical trials, revised as E6(R3), with Annex 2 adopted in June 2026.
IEC 62304
OfficialIEC 62304 Medical Device Software: Software Life Cycle Processes
IEC international standard for medical device software life cycle processes; the current text is the 2006 edition plus Amendment 1 (2015).
IEC 62366-1
OfficialIEC 62366-1 Medical Devices: Application of Usability Engineering
IEC standard for applying usability engineering to medical devices to reduce use-related risk. Current: IEC 62366-1:2015+AMD1:2020.
ISO 13485
OfficialISO 13485:2016 Medical Devices Quality Management Systems
International standard from ISO setting quality management system requirements for organizations involved in the medical device life cycle.
ISO 14001
OfficialISO 14001 Environmental Management Systems
ISO 14001:2026 is the ISO standard specifying requirements for an environmental management system, with guidance for use.
ISO 14971
OfficialISO 14971:2019 Medical Devices: Application of Risk Management to Medical Devices
ISO international standard for risk management across the life cycle of medical devices, including in vitro diagnostic devices; third edition 2019.
ISO 28000
OfficialISO 28000 Security and Resilience: Security Management Systems
ISO 28000:2022 is the ISO standard specifying requirements for a security management system, including aspects relevant to the supply chain.
ISO 9001
OfficialISO 9001 Quality Management Systems: Requirements
ISO international standard setting requirements for a quality management system. Current edition: ISO 9001:2026.
ISO/IEC 27001
OfficialISO/IEC 27001 Information Security Management Systems
ISO/IEC 27001:2022 is the ISO and IEC standard specifying requirements for an information security management system (ISMS).
ISO/IEC 27017
OfficialISO/IEC 27017 Information Security Controls Based on ISO/IEC 27002 for Cloud Services
ISO/IEC guidance on information security controls for cloud service providers and customers, based on ISO/IEC 27002. Current edition: 2026.
ISO/IEC 27018
OfficialISO/IEC 27018:2025 Protection of PII in Public Clouds
ISO/IEC guidelines for protecting personally identifiable information in public clouds where the provider acts as a PII processor. 2025 edition.
MDSAP
OfficialMedical Device Single Audit Program (MDSAP)
MDSAP lets one recognized auditing organization audit a device maker for the FDA, Health Canada, TGA, ANVISA and Japan's MHLW and PMDA.
NIST CSF 2.0
OfficialNIST Cybersecurity Framework (CSF) 2.0
NIST guidance for managing cybersecurity risk, organized into six functions: Govern, Identify, Protect, Detect, Respond and Recover.
PCI DSS
OfficialPayment Card Industry Data Security Standard (PCI DSS)
PCI Security Standards Council standard for protecting payment account data wherever it is stored, processed or transmitted. Current: v4.0.1.
PCI DSS
OfficialPCI Data Security Standard (PCI DSS) for Healthcare Payments
PCI Security Standards Council standard for protecting payment card data, current version v4.0.1, applying to any entity handling card data.
RDM and FAIR
OfficialResearch Data Management and FAIR Principles
Research data management and sharing practices, including the FAIR principles and the NIH Data Management and Sharing Policy for NIH-funded work.
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