QUANTIFY RESEARCH is a global partner to the pharmaceutical industry in close partnership with academia, patients, public institutions & clinical experts.
Real-world evidence & analytics
Quantify is the leading provider of RWE generated from the world-renouned Nordic data. Through our local presence, expert staff, institutional know-how and more than 10 years’ hands-on experience with the Nordic data, we offer an unparalleled ability to advise and execute Nordic RWE studies with local and global applications. Quantify has a successful track record of advising clients on securing Nordic ethical approval, data access, and optimizing analysis for commercial or regulatory purposes. We also offer RWE services in the EU, UK, and US.
Modelling, Access & Strategy
Quantify is a global provider of health economic evidence and a specialist provider of Nordic market access services including economic models, reimbursement dossiers, and strategic advice. Our experience and expertise ensures an optimized, streamlined market access process across the Nordics. For non-technical stakeholders, Quantify also develops value tools and visualisation dashboards to enhance communication. Our expert staff include ex-payers, ex-pharma, modelling experts, and experienced project managers.
Evidence review & synthesis
Quantify has long standing experience reviewing, interpreting and communicating evidence as part of targeted or systematic literature reviews (SLR). Our team ensures these activities are done systematically, with a focus on usability, to support knowledge management and commercialization activities. QUANTIFY is experienced in summarizing the results of this work through meta-analyses and narrative reviews. Our team consists of 50% PhDs and integrated AI solutions to provide our clients with the very best services.
Press
Use Cases for Literature Reviews Across the Pharmaceutical Product development Lifecycle
Literature reviews are essential throughout the pharmaceutical product development lifecycle, from identifying therapeutic targets to assisting with regulatory and health technology assessment submissions and ultimately improving drug safety and patient outcomes at every stage.
This image presents the use cases for literature reviews across the life cycle of product development, something our Evidence Review and Synthesis team are experts in!
Driving innovation in Nordic SLD research🔍
Last week, Quantify’s Emilie Toresson Grip was invited to the first Swedish Steatotic Liver Disease (SLD) Think Tank, hosted by Karolinska Institutet.
24 hours packed with speed networking, group discussions, and insightful presentations.
The primary goals? Strengthening existing networks and fostering new connections across academia and industry.
The ultimate objective was to elevate Sweden and the Nordic countries’ position in international SLD research.
It’s an exhilarating time […]
Quantify is excited to attend the DIA RWE conference in Philadelphia!
Our CEO Kirk Geale, PhD will be attending the DRUG INFORMATION ASSOCIATION (DIA) Real-World Evidence conference in Philadelphia from October 24-25, 2024!
We are looking forward to meeting with clients and partners to showcase how our unique Nordic data can support global and US stakeholders with relevant and reliable RWE. Our highly transportable data has the power to answer research questions that […]
Health Economics Conference 2024 in Norway
Last week Quantify Research was present at the annual Health Economics Conference (Helseøkonomikonferansen) in Norway.
The conference gathered a broad audience and participation from academia, the healthcare sector, industry, patient organisations and government.
Over two days, the program was packed with presentations and discussions about hospital waiting times, the GP service, uncertainty and documentation in economic evaluation, perspectives and prioritisation in decision making, large public […]