Cross-market B2B research is only reliable if the quality framework is consistent across every geography. We run the same multi-stage quality validation in Tokyo as in Toronto.
The typical approach to global panel coverage is partnership aggregation: buy from local providers in each market, stitch the data together, present it as a unified panel. The quality framework varies by supplier. The documentation varies. The verification depth varies. You find this out when you try to make comparisons across markets and the data doesn't hold up.
Our global research panel applies the same sampling logic, the same identity verification protocols, and the same acceptance criteria across all 90+ markets. Regional compliance (GDPR, CCPA, PDPA, PIPL) is handled at the market level — the quality framework doesn't change.
Read the Methodology →US and Canada with state/province-level targeting. CCPA and PIPEDA-compliant consent management. The deepest verification coverage in our global portfolio.
UK, Germany, France, Netherlands, Nordics, and 20+ additional European markets. GDPR-compliant with DPA capability in all EU/EEA markets. ICO registered for UK studies.
Australia, Japan, Singapore, India, South Korea, and 13 additional APAC markets. PDPA and PIPL-aware protocols. Local-language survey capability where needed.
Brazil, Mexico, Colombia, Argentina, Chile, and additional LATAM markets. Portuguese and Spanish survey capability. LGPD-compliant data handling for Brazilian studies.
UAE, Saudi Arabia, South Africa, Nigeria, and select additional markets. Coverage depth varies — we give you an honest feasibility assessment before any commitment.
Cross-market studies use the same questionnaire logic and validation framework in each market, ensuring data is genuinely comparable rather than just co-fielded.
Compliance isn't a checkbox we apply at the end. It's built into how consent is collected, how data is processed, and what's documented in your quality audit.
Explicit consent under Art. 6(1)(a). Timestamp and consent-version records. DPA available for all EU/EEA studies. ICO-registered for UK. Supervisory authority registration in DE, FR, NL.
Opt-in consent with right-to-delete capability. No sale of personal information without explicit consent. Documented consumer request response process.
Market-specific consent frameworks for Singapore PDPA, China PIPL, India DPDP, South Korea PIPA. Local counsel review for all APAC data processing agreements.
Standard contractual clauses (SCCs) for EU-to-non-adequate-country transfers. Transfer impact assessments available on request for regulated industries.
Tell us which markets, what professional target, and your timeline. We'll give you market-level feasibility estimates and flag any markets where coverage depth is limited.