Breaking down barriers: increasing diversity in clinical trials
Introduction Clinical trials are the cornerstone of medical advancements. They provide the critical data needed to develop new treatments and improve patient outcomes. […]
Driving insights into neurological diseases through data
Introduction Gathering sufficient data to drive new insights on drug targets and therapies poses a significant hurdle in addressing human illnesses. Nowhere […]
Integration of germline data in precision medicine
Introduction Precision medicine, a groundbreaking approach tailoring medical treatment to an individual’s characteristics, has revolutionized healthcare. However, its full potential is yet […]
Utilizing oncological data in discovery and validation
Introduction In the realm of oncology, data is a powerful tool. It holds the potential to revolutionize cancer treatment and patient outcomes. […]
Current US regulatory guidance on using real world data in research and clinical trials
Introduction Real world data and evidence (RWD/E) are becoming increasingly important in the healthcare industry. RWD is collected from sources outside of traditional […]
Challenges of using real world data in research and clinical trials
Introduction Patient and health information obtained outside of clinical trial settings is referred to as real world data (RWD). Analyzing RWD leads to […]
Preserving Patient Data Privacy and Security in the Face of Cyber Attacks
Recent cyber attacks targeting major U.S. health organizations underscore the critical importance of safeguarding sensitive patient and public health data. With each […]
The benefits of leveraging real world data and evidence in clinical research and trials
Introduction What is Real World Data (RWD) and Real World Evidence (RWE)? Real world data (RWD) encompasses information gathered beyond clinical trial […]
Unlocking insights: how real world data is shaping clinical research and trials
Introduction Clinical trials are a vital stage in the drug development process and are used to evaluate the safety and effectiveness of […]
Facilitating the establishment of high-quality patient registries
Patient registries are essential tools for collecting and analyzing data on specific diseases, conditions, or treatments. They provide valuable insights into patient outcomes, […]
Four key benefits of using patient registries to progress rare disease insights
Rare diseases impact between approximately 250-450 million people globally, but they often receive less attention and funding than more common diseases. This can […]
Creating research-ready data from 135,000 cancer, rare disease & COVID-19 participants
Introduction Around the world, organisations across the healthcare system produce huge quantities of information about patients, diseases, and treatments. Highly sensitive and […]