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Regulatory Governance & Data Trust

Global Compliance & Research Ethics

Strict adherence to ISO 20252:2019, ISO 9001, GDPR, HIPAA, ESOMAR, MRSI, and EphMRA international market research standards. Protecting client confidentiality and respondent privacy with cryptographic provenance.

ISO 20252:2019 Certified EU & UK GDPR Article 5 EphMRA Code Aligned SOC 2 Type II Aligned
Cryptographic Security & Data Privacy Architecture
CRYPTOGRAPHIC DATA VAULT
AES-256 / TLS 1.3 SOVEREIGN ENCRYPTION
Institutional Accreditations

Global Certification Matrix

Audited compliance frameworks governing every phase of respondent recruitment, data transfer, and final reporting.

ISO 20252:2019 Core Standard

Market & Social Research Standard

International standard establishing rigorous quality management, transparency, sample traceability, and standardized execution across all quantitative and qualitative fieldwork operations.

Annual Independent Audit
ISO 9001:2015 Quality Management

Operational Quality Framework

Total quality management standard guaranteeing continuous process improvement, stakeholder risk assessment, systematic corrective action loops, and service delivery consistency.

Certified Operations
EU & UK GDPR Data Sovereignty

Privacy & Data Rights Charter

Full compliance with Articles 5, 6, and 9 of GDPR and India DPDP 2023. Explicit triple opt-in, strict purpose limitation, zero commercial re-targeting, and guaranteed 72-hour Right to be Forgotten (RTBF) SLA.

One-Way SHA-256 PII Hashing
ESOMAR Corporate Member

ICC/ESOMAR International Code

Strict adherence to the global ethical code of conduct governing respondent privacy, research transparency, objective reporting, and full ESOMAR 37 disclosure transparency for panel buyers.

ESOMAR 37 Disclosures
MRSI Accredited Member

Market Research Society of India

Corporate member aligned with MRSI ethical standards, promoting rigorous fieldwork auditing, fair respondent compensation models, and professional excellence across the APAC region.

Corporate Accreditation
EphMRA & HIPAA Healthcare Ethics

Pharmaceutical & HCP Standards

European Pharmaceutical Market Research Association compliance including mandatory 24-hour Adverse Event (AE) reporting protocols, physician confidentiality shields, and HIPAA Safe Harbor de-identification.

24-Hr Adverse Event Protocol
Data Protection Architecture

Four Pillars of Research Governance

Engineering privacy directly into the data collection and distribution lifecycle.

PILLAR 01

Sovereign Cloud Silos

Regional data storage silos in Frankfurt (EU), London (UK), Virginia (US), and Mumbai (APAC) ensuring data never leaves sovereign jurisdiction without explicit authorization.

PILLAR 02

Explicit Triple Opt-In

Every panel participant undergoes multi-factor email and SMS identity verification. No scraped lists, no purchased third-party cohorts, zero cold contact.

PILLAR 03

Pharmacovigilance AE Gate

Standard Operating Procedure (SOP) ensuring any spontaneous Adverse Event disclosed during healthcare fieldwork is forwarded to client pharmacovigilance teams within 24 hours.

PILLAR 04

Cryptographic Provenance

Delivered datasets include immutable verification tokens proving complete absence of synthetic bot traffic, speeders, or duplicate session manipulation.

Legal & Privacy Desk

Request a Data Processing Addendum (DPA)

Our legal and compliance team provides enterprise-tailored Data Processing Addendums (DPAs), Standard Contractual Clauses (SCCs), Business Associate Agreements (BAAs), and mutual non-disclosure agreements within 4 business hours.

Data Protection Officer: dpo@scrutinyglobal.com