1,348 件 ・ 関連度順
概要と使いどころ
Implements the GDPR Article 17 right to erasure (right to be forgotten) workflow, covering all six grounds for erasure, five exceptions, technical deletion versus anonymization decisions, and third-party notification under Article 19. Activate for erasure request, deletion request, right to be forgotten, Art. 17 queries.
日本語の概要は準備中です。原文の説明を表示しています。
Implements NIST SP 800-88 Rev. 1 media sanitization procedures including Clear, Purge, and Destroy methods for all media types. Covers certificate of destruction generation, verification procedures, vendor management for third-party destruction, and chain of custody documentation. Activate for data destruction, media sanitization, secure erasure, certificate of destruction queries.
日本語の概要は準備中です。原文の説明を表示しています。
Creates GDPR Article 30(2) Records of Processing Activities for data processors with all four mandatory fields: processor and controller names and contact details, categories of processing, third country transfers, and security measures description. Activate for processor RoPA, Art. 30(2), processor records, sub-processor documentation.
日本語の概要は準備中です。原文の説明を表示しています。
Audits Records of Processing Activities against supervisory authority templates from CNIL, ICO, and BfDI. Provides completeness scoring, gap identification, and remediation tracking. Activate for RoPA audit, completeness check, supervisory authority readiness, CNIL template, ICO template, BfDI template, gap analysis.
日本語の概要は準備中です。原文の説明を表示しています。
Implements HIPAA breach notification requirements under 45 CFR §164.400-414. Covers individual notification within 60 days, HHS reporting thresholds (500+ immediate, under 500 annual), state attorney general notification, media notification for 500+ in a state, and breach risk assessment. Keywords: HIPAA breach notification, HHS reporting, OCR breach portal, individual notice, state attorney general.
日本語の概要は準備中です。原文の説明を表示しています。
Guides the three-part Legitimate Interest Assessment (LIA) required under GDPR Article 6(1)(f): purpose test, necessity test, and balancing test. Activate when evaluating legitimate interest as a lawful basis, conducting LIA reviews, or documenting proportionality analysis. Keywords: LIA, legitimate interest, balancing test, necessity test, purpose test, Article 6(1)(f).
日本語の概要は準備中です。原文の説明を表示しています。
Guides DPIA for health and medical data processing covering Art. 9(2)(h)-(j) exemptions, HIPAA crosswalk for transatlantic operations, clinical trial data protection under EU CTR 536/2014, and genetic data specifics under Art. 9(1). Activate for healthcare systems, clinical research, health apps, or medical device data. Keywords: health data, DPIA, Art. 9, clinical trial, genetic data, HIPAA, medical records, special category.
日本語の概要は準備中です。原文の説明を表示しています。
Decision framework for choosing between consent and legitimate interest as the lawful basis for processing. Covers power imbalance indicators, conditionality prohibition under Article 7(4), granularity requirements, the three-part LIA test (purpose, necessity, balancing), and practical decision trees for common scenarios.
日本語の概要は準備中です。原文の説明を表示しています。
Manages the absolute right to object to direct marketing under GDPR Article 21(2)-(3), covering immediate cessation of all direct marketing processing, suppression list management, cross-channel enforcement, and profiling for marketing purposes. Activate for marketing opt-out, unsubscribe, Art. 21(2), direct marketing objection queries.
日本語の概要は準備中です。原文の説明を表示しています。
Guides compliance with Japan's Act on the Protection of Personal Information (APPI, 2022 amendments). Covers individual rights expansion, cross-border transfer restrictions including pre-transfer information requirements, PPC enforcement, and pseudonymised and anonymously processed information. Keywords: APPI, Japan data protection, PPC, cross-border transfer, pseudonymised information, individual rights.
日本語の概要は準備中です。原文の説明を表示しています。
Guides determination of the correct lawful basis under GDPR Article 6(1)(a)-(f) for each processing activity. Includes decision tree logic for consent vs legitimate interest vs contract necessity. Activate when evaluating legal grounds for processing or reviewing lawful basis selections. Keywords: lawful basis, Article 6, consent, legitimate interest, legal obligation, contract.
日本語の概要は準備中です。原文の説明を表示しています。
Guides compliance with South Korea's Personal Information Protection Act (PIPA, 개인정보 보호법). Covers pseudonymisation framework, notification requirements, PIPC enforcement, consent standards, and cross-border transfer rules under the 2023 amendments. Keywords: PIPA, Korea data protection, PIPC, pseudonymisation, consent, cross-border transfers.
日本語の概要は準備中です。原文の説明を表示しています。
Guide for managing consent for scientific research under GDPR Article 89 and Recital 33 broad consent provisions. Covers ethical review board coordination, purpose evolution management, appropriate safeguards including pseudonymization, and the interplay between consent and other lawful bases for research processing.
日本語の概要は準備中です。原文の説明を表示しています。
Guide for managing consent for children's personal data under GDPR Article 8 and COPPA. Covers parental consent mechanisms, age verification methods, country-specific age thresholds (ranging from 13 to 16), parental authorization workflows, and age-appropriate design per the UK ICO Children's Code.
日本語の概要は準備中です。原文の説明を表示しています。
Conducts HIPAA risk analysis per 45 CFR §164.308(a)(1) following OCR guidance methodology. Covers threat identification, vulnerability assessment, likelihood and impact determination, risk scoring, and mitigation planning for electronic protected health information. Keywords: HIPAA risk analysis, OCR guidance, threat assessment, vulnerability, risk management, ePHI.
日本語の概要は準備中です。原文の説明を表示しています。
Guides compliance with India's Digital Personal Data Protection Act 2023. Covers consent manager registration, data fiduciary obligations under Sections 4-7, significant data fiduciary requirements under Section 10, data principal rights, and Board enforcement framework. Keywords: DPDP Act, India data protection, consent manager, data fiduciary, significant data fiduciary, data principal rights.
日本語の概要は準備中です。原文の説明を表示しています。
Manages legal hold and data preservation processes including triggering events, custodian notification, hold-in-place technical implementation, release procedures, and interaction with retention schedules. Covers litigation hold registers, compliance monitoring, and Art. 17(3)(e) exception documentation. Activate for legal hold, litigation preservation, data freeze, e-discovery hold queries.
日本語の概要は準備中です。原文の説明を表示しています。
Implements HIPAA minimum necessary standard under 45 CFR §164.502(b). Covers role-based access policies per workforce member category, routine vs non-routine disclosure protocols, reasonable reliance doctrine, documentation requirements, and HITECH amendments. Keywords: minimum necessary, role-based access, workforce, routine disclosure, HIPAA.
日本語の概要は準備中です。原文の説明を表示しています。
Executes breach notification under HIPAA Breach Notification Rule (45 CFR 164.400-414). Covers 60-day individual notification, HHS/OCR reporting for breaches of 500+ individuals (immediate) and under 500 (annual log), state attorney general notification, media notification for 500+ in a single state, and breach risk assessment using the four-factor test. Keywords: HIPAA, breach notification, PHI, HHS, OCR, covered entity, business associate.
日本語の概要は準備中です。原文の説明を表示しています。
Conducts comprehensive inventory of protected health information across the enterprise per HIPAA Security Rule requirements at 45 CFR §164.308(a)(1)(ii)(A) and §164.310(d). Covers identification of all ePHI repositories, data flow mapping, classification of PHI by sensitivity, and integration with risk analysis. Keywords: PHI inventory, ePHI, data mapping, information asset, data flow, HIPAA risk analysis, designated record set.
日本語の概要は準備中です。原文の説明を表示しています。
Guides the establishment and management of joint controller arrangements under GDPR Article 26, including determination of joint controllership, allocation of responsibilities, and transparency obligations. Activate when two or more controllers jointly determine purposes and means of processing, or when evaluating shared data platforms. Keywords: joint controller, Article 26, shared responsibility, arrangement, joint determination.
日本語の概要は準備中です。原文の説明を表示しています。
Manages HIPAA Business Associate Agreements under 45 CFR §164.502(e) and §164.504(e). Covers required BAA provisions, business associate vs subcontractor obligations, breach notification chain, downstream BA requirements, and termination remedies. Keywords: BAA, business associate, subcontractor, HIPAA compliance, PHI disclosure, termination.
日本語の概要は準備中です。原文の説明を表示しています。
Implements HIPAA Security Rule technical safeguards under 45 CFR §164.312 for electronic protected health information. Covers access controls with unique user identification, emergency access procedures, automatic logoff, encryption, audit controls, integrity controls, and transmission security. Keywords: HIPAA Security Rule, ePHI, access controls, encryption, audit controls, technical safeguards.
日本語の概要は準備中です。原文の説明を表示しています。
Manages RoPA for complex multi-entity corporate groups including entity-level versus group-level records, intra-group transfer documentation, and shared processing coordination. Activate for group RoPA, multi-entity, corporate group, intra-group transfers, subsidiary records, holding company.
日本語の概要は準備中です。原文の説明を表示しています。