Providing global and local expertise in Medical Affairs.
Real World Data (RWD) is increasingly seen as a trusted source for healthcare decision-making and a wide range of key stakeholders are embracing and validating its use. Our team of local experts, backed by extensive Real World Data, help you navigate the complexities of the healthcare industry. Whether it's strategic planning or adapting to market dynamics, our specialized knowledge equips you to make well-informed decisions. We offer valuable insights into the preferences of regulators, payers, and patients, providing essential support to life sciences organizations at every stage of the product life cycle.
With dedicated teams in each Nordic country, IQVIA delivers tailored support for evidence and RWD planning, addressing the unique requirements of local affiliates, headquarters, and public healthcare entities.
IQVIA has local staff in every Nordic country to support planning, access, management and analysis of RWD. Our local staff are for data access experts, epidemiologists, statisticians, data scientists, and project leads have extensive experience in navigating the complex data landscape.
Studies can be performed as single or multi-country studies. For more complex studies, secondary RWD databases need to be enriched with more specific data from primary data generation (such as chart reviews, EMRs, or patient-generated data). IQVIA specializes in these hybrid studies and can support researchers in feasibility and study implementation.
Nordics encompass one of the most richest real world data ecosystems in Europe, with unparalleled registry data that is linkable and has long follow-up. We at IQVIA can help pharmaceutical companies and healthcare organizations navigate to success and is open to discussing collaborations and partnerships.
Our Clinical Operations team is dedicated to the success of your clinical trials. Our highly experienced team provides comprehensive support, from planning and design to execution and monitoring, ensuring the highest quality standards.
We offer tailored services, including feasibility studies, regulatory submissions, site management, and monitoring, to meet your specific needs. Our team is well-versed in Good Clinical Practice and regularly trained in the latest guidelines and policies.
With a global reach and local presence, we ensure exceptional oversight and management. A local CRA will be your single point of contact throughout the study, providing consistent and reliable support from start to finish.
Our team of data access experts, epidemiologists, statisticians, data scientists, and project leads has extensive experience regulatory grade RWE. Increasingly, regulatory authorities are seeing the value of real world evidence (RWE) to evaluate a product’s safety and effectiveness. This changing environment presents you with new opportunities to increase the effectiveness and efficiency of your safety and regulatory studies.
We are committed to driving innovation and excellence in our industry. Our thought leadership initiatives bring you the latest insights, trends, and expert analyses to help you stay ahead of the curve.
Tel: +45 70 27 70 01
Espoo
Turku
Tel: +358 (0)9 4241 3800
Stockholm
Postal Address:
Hagaplan 4
113 68 Stockholm
Hagaesplanaden 49
113 68 Stockholm
Tel: +46 8 50 88 42 00
Mölndal (Gothenburg)
Prästgårdsgatan 28
431 44 Mölndal