Extensive article today in the Swedish newspaper Dagens Nyheter on the increasing burden of fatty liver disease (NAFLD), including an interview with Associate Professor Hannes Hagström, co-creater of the HERALD liver data platform together with Quantify Researchs Emilie […]
Quantify Research recently joined regulators and industry in the EMA’s Multi-stakeholder workshop on Real World Data (RWD) quality and Real World Evidence (RWE) use.
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Studying rare diseases in real-world evidence often comes with challenges, such as lack of disease-specific diagnosis codes and complex definition of relevant endpoints. Over the years, Quantify has faced these challenges on […]
Denmark, through the Danish Medicines Council, will join FINOSE! We at Quantify foresee that this can potentially be a great preparation for both HTA bodies and pharmaceutical manufacturers for the upcoming EU HTA regulation. The addition of Denmark to FINOSE […]
The Quantify team has had a fantastic first day at #isporannual! Today’s schedule was full with many meetings and interesting program sessions.
One thing is clear – Nordic RWD has great […]
Will you be attending #ISPOR in #Boston next week? Quantify’s Kirk Geale, Emilie Toresson Grip & Puneet Kaushik will be on site and ready to connect at #ISPORAnnual! Keep a lookout for booth […]
The NPF has recently published a new strategy aiming to strengthen the collaboration between the Nordic countries. New, innovative and advanced therapies can offer hope and cure for patients, however it […]
Are you looking for a partner to provide support in Nordic HTA submissions? QUANTIFY is a true pan-Nordic vendor with hands-on expertise in all Nordic countries combined with experience developing Global HEOR material, in addition to local offices and in-house […]
Quantify Research will attend this year’s annual SHEA-conference (Swedish Health Economic Association) in Stockholm on Tuesday and Wednesday (April 25th-26th). Our Nordic HTA experts Lena Jacobs, Hannah Norman and Konstantin Macheridis will participate in this […]
We had a great time at the Nordic Rare Disease Summit 2023 last week, where important topics such as early diagnosis, patient empowerment, access to innovative treatments and EU legislation were discussed. […]