Post-Brexit, the UK is now a distinct regulatory and market access jurisdiction. Global teams that exclude UK data are missing a critical data point.
Post-Brexit, MHRA operates independently of EMA. UK approval timelines and label differences directly affect global market access strategy.
NICE appraisals are globally benchmarked. Payers worldwide reference NICE cost-effectiveness decisions. UK HCP insight on NICE outcomes is uniquely valuable.
10,000+ verified UK HCPs across all specialties — rapid fieldwork completion with high-quality, low-dropout respondents.
NHS OpenPrescribing data gives UK HCP responses unique context for formulary and prescribing behaviour research.
UK fieldwork typically completes in 2–4 working days — often faster than any EU5 market — allowing rapid insight for global timelines.
GMC-verified panel with professional email validation. No panel pollution, no fraudulent responses common in open-access panels.
From rapid quantitative surveys to multi-country advisory boards — scoped and executed to global pharma standards.
UK + EU5 quant surveys with harmonised questionnaires, parallel fieldwork, and unified analysis. Typical n=50–200 per country.
IDIs with key opinion leaders, prescribers and specialists across UK and European markets. Multilingual moderation available.
Virtual advisory panels with 6–12 HCPs across UK + EU. Full facilitation, verbatim reporting, and EFPIA-compliant honoraria management.
Test brand positioning, IVAs, patient materials and messaging with HCPs across multiple markets before global launch.
Treatment algorithm mapping, competitive intelligence, and unmet need assessments across UK and European markets.
HCP perspectives on cost-effectiveness, payer value messaging, and access barriers — aligned to NICE, HAS, IQWIG and other HTA bodies.
ClinicaliQ leads UK fieldwork and coordinates with established HCP research partners across Europe — one brief, one commercial relationship, one report.
We can provide a full compliance summary for your procurement or legal team before project commencement.
Request Compliance PackTell us your research objectives and target markets. We'll respond with a scoped proposal and indicative pricing within 24 hours.
Get weekly clinical updates — guidelines, trials, MHRA alerts — delivered to your inbox. Free for verified HCPs.
By registering you confirm you are a healthcare professional. No spam. Unsubscribe anytime.