What's new

With data starting in 2022, Close-Up's Non-Retail Pharma Market Prescription Data On Physician Level for Drugs provide a mapping of product performance in the market by indication and treatment line. The audit is designed to serve the market of "High Cost" products, which cover therapeutic areas such as oncological pathologies, autoimmune diseases, "rare" diseases, etc.

Established as an informal group in 1983 and becoming a society in 1994, the European Society for Immunodeficiencies (ESID) is a non-profit organization with data across several countries of Europe whose main objectives are to facilitate the exchange of ideas and information among doctors, nurses, biomedical investigators, patients and their families concerned with primary immunodeficiency disease

The Swedish National Parkinson's Disease Patient Registry (PARKreg) is a national quality registry that aims to contribute to Swedish Parkinson's care by spreading new knowledge through research and education. Established in 2010, the register currently covers approximately 15,681 people with Parkinson's (PwP), out of whom 10,735 are still alive and residing in Sweden (of an estimated total of 22,000 PwP).

Whether you're a seasoned user or just getting started, these tutorials are tailored to help you get started on our platform effortlessly. Each video breaks down the process step-by-step, empowering you to optimize your experience and achieve your goals faster.

It’s been a busy week for us. We continue to bring you descriptions of more new healthcare databases worldwide and welcome requests for specific ones you want us to include in our resource. Check out the latest two we just finished profiling:

These EXPLORE-LC datasets consist of inpatients and outpatients diagnosed with NSCLC (Non-Small Cell Lung Cancer). Data are currently available for the periods of 2014-2020 for Australia and Korea, and 2016-2021 for Taiwan -

Check out the 5 profiles we just added to our resource:

The IQVIA Hepatocellular Carcinoma (HCC) Disease Registry database is available in nine Asia-Pacific countries: Australia, China, Hong Kong, Japan, New Zealand, Republic of Korea, Singapore, Taiwan, and Thailand. The HCC Disease Registry is a consented prospective data collection (with retrospective lookback to time of diagnosis) for HCC patients. Data are captured using e-CRF / site-based approach since January 2013. 

Close-Up: NON-RETAIL PHARMA (Market Sales Data Institution Level) databases contain two years (Moving Annual Total) worth of sales information captured via a panel of providers formed by wholesalers working in the non-retail channel. It includes information at the Institution Level on all laboratories, molecules, therapeutic classes, categories, and pharmaceutical forms for Rx and OTC products.

How long have you waited to try out B.R.I.D.G.E. TO DATA^® for just 30 days? Based on several requests, we decided to let you and four other colleagues at your organization access ~450 database / registry profiles from 63 countries for one month; if you like it, pay the difference and access it all year round by just paying the difference of an annual subscription.