

Answer crucial clinical, regulatory and commercial questions with Real World Evidence approaches
Real world data (RWD) and RWE refer to any relevant patient-level data not collected through a typical, most often randomized, clinical trial (RCT). Clinical trials are usually designed to prove whether a medicine or treatment works under specific conditions and as such have a large number of inclusion and exclusion criteria. This limits the number of patients eligible for the clinical trial and the generalizability of the trial’s results to the other patients with the disease of interest.
RWE adds perspective to RCT results by offering a granular view of the patient journey and treatment experience in the real world. These observations can be gathered from a variety of non-interventional sources, including data from routine hospital or doctor visits, patient registries, claims reports, connected devices, prescription data, observational studies, and other primary and secondary patient-level data.
A proven partner with trusted expertise
IQVIA APAC Real World Solutions (RWS) team is the proven partner for the right RWE to meet stakeholder needs throughout the end-to-end product life cycle, from clinical development to launch and post-launch stages.
We are a one-stop RWS provider, with 4 key offerings supported by multiple study approaches. Each study approach has its respective implications and considerations such as timeline, data availability and country-specific factors. Having housed all solutions under one umbrella, we are able to achieve innovation and synergy across approaches, offering clients with the optimal study design to answer your key research questions. Reach out to our RWS experts to help you identify the best approach to answer your key research questions.
Evidence Generation Strategy & Medical Consultancy Services
- Educational programs
- Scientific workshops
- Integrated evidence generation strategy
- KOL mapping
- Medical advisory services
Real World Evidence Generation
- Secondary database research, e.g., electronic medical records (EMR), claims and existing registries
- Prospective and retrospective non-interventional study, e.g., post-marketing surveillance, retrospective chart review and patient registry
- Clinical cross-sectional surveys, e.g., physician survey, patient surveys and patient reported outcomes
- Hybrid-study or mixed methods, e.g., mosaic study
- Qualitative studies
Health Evidence (HE) & Health Technology Assessment (HTA) Related Services
- HE modelling – cost-effectiveness analysis (CEA), budget impact analysis (BIA)
- Comparative effectiveness – systematic literature review (SLR), meta-analysis (MA) and network meta-analysis (NMA)
- Pricing, reimbursement and HTA consultancy services
- Market access
- HTA dossier preparation
Evidence Dissemination
- Medical and scientific communication
- Evidence dissemination strategic plan
Leverage deep domain expertise from our team of experts
Site-based Research
Secondary Database Studies
Health Economics & Outcomes Research (HEOR)
Expertise where it counts
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Our Experience in Site-based Research
200+ Studies
conducted in the last five years across Asia Pacific
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Our Coverage in Site-based Research
70,000+ Patients
enrolled across 7,000+ sites in the last five years throughout Asia Pacific
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Our Experience in HEOR
250+ HEOR Projects
across multi-countries in Asia Pacific in the last five years
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Our Expertise in HEOR
140+ HEOR Publications
including journal and academic conference presentations in the last five years
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Our Experience in Secondary Database Studies
150+ Projects
across multi-countries in Asia Pacific in the last three years
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Our Expertise in Secondary Database Studies
110+ Publications
based on secondary database research including journal and academic conference presentations in the last three years
