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Home > All articles > Setting up a Nordic RWE study in Sweden – fast access to patients’ numbers and distribution across Sweden
Setting up a Nordic RWE study in Sweden – fast access to patients’ numbers and distribution across Sweden
Sweden’s publicly funded healthcare system and universal access to specialized health care make the data derived from Sweden broadly generalizable, covering diverse populations including different ethnic backgrounds.
The wealth of population-level health and administrative data in Sweden, often reaching nearly 100 percent coverage with high concordance, serves as a valuable resource to pharmaceutical companies for real-world evidence (RWE).
The ability to unambiguously link data from various sources over time using the unique Swedish identity number enhances the richness of datasets. With data ownership spread across national and regional databases, disease-specific quality registries, hospital-level data, biobanks, and researcher-generated databases, Sweden offers abundant opportunities for registry-based RWE studies. In particular, having in-depth hospital-level data is a valuable asset, facilitating the possibility of building well-designed external control arms.
Sweden is a highly dynamic environment for RWE studies in Nordic
Swedish registers also provide information on administrative data such as pricing of pharmaceuticals and medical operations. The readily available data on sick leaves with ICD-10 codes and socioeconomic factors enables exploration of illness-related leave from work, patients’ educational backgrounds, household income, etc.
“Sweden is a highly dynamic environment aiming to continuously keep its position among the top and to develop into a globally leading RWE generation country for pharma market, innovation and research. Therefore, monitoring Sweden’s progress closely is advisable for pharma companies”, says Medaffcon´s Lead RWE epidemiologist Johanna Simin.
An excellent partner for mapping the Swedish market is Medaffcon, a pioneer in RWE and biobank research in Finland. Its expertise now extends to registry research in Sweden.
Medaffcon’s strengths as a partner for RWE studies in Nordic countries:
Highly experienced health economics, market access, and RWE professionals as experts
Experts with backgrounds from leading positions in pharmaceutical companies. Excellent understanding of the needs and business perspectives of the pharmaceutical industry in RWE studies
Experts with broad academic backgrounds and current academic affiliations to continuously strengthen the scientific perspective of RWE projects
A strong data analysis team dedicated to applying state-of-the-art methods for data analysis in RWE studies
Experienced professionals evaluating that the data is fit for purpose and suitable for the objectives, facilitating the possibility of drawing meaningful inferences from the obtained results
Experienced professionals who can strategically guide projects of pharmaceutical companies based on their insights to ensure optimal utilization of data
High capacity to conduct projects (i.e., timely delivery, start ASAP, etc.)
The Nordic countries provide an excellent environment to assess market access opportunities for pharma industry. In Sweden and Finland, a pharma company can quickly and smoothly determine the number of patients, the standard of care, the products of competitors in the market, their weaknesses and limitations, as well as where competitors’ products are used.
Fast access for pharma companies to Nordic RWE data
Aggregate-level national real-world evidence (RWE) data in Sweden can be obtained in 1-5 days. Ethical approval is not required. The data includes:
Number of patients
Gender distribution
Age distribution
Place of residence/region (geographical distribution)
Top 20 diagnoses (in- and outpatient care)
Top 20 prescription drug usage
Prescriber information
Top 20 surgical procedures
With this information, clients can make decisions about market entry very quickly. Fast access also rapidly provides the information needed for discussions with authorities regarding ongoing market access processes.
Lisse-Lotte started at Medaffcon 1st of October 2024. Previously she was at a Swedish-German company as CSO Chief Scientific Officer, consulting European companies about Nordic health data opportunities and market access. She has a M.Sc (Econ.) from Helsingin School of Economics and a M.Sc (Health Econ) from Karolinska. Additionally a Ph.D student at the University of Turku in Health Economics. She has obtained a long experience from global pharma and medtech. She has lived over 20 years in Sweden.
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