Learn more about Lindus Health from our blog page. Our posts cover an array of topics from clinical developments to diversity.
The global in vitro diagnostics (IVD) market is evolving rapidly, driven by growing demand for faster, more accessible testing across clinical and consumer settings. As healthcare systems shift toward earlier detection, personalised treatment, and decentralised care, the need for innovative diagnostics has never been greater.
Psychedelics are reshaping mental health treatment, with over 100 active psilocybin trials reflecting renewed interest after decades of stalled progress due to stigma and regulation.
The transition from IVDD to IVDR represents the most significant regulatory change for diagnostic devices in Europe in decades. With extended transition periods now in place, clinical study sponsors face both new challenges and opportunities. Understanding the evolving requirements is essential to staying compliant and keeping studies on track.
The continuous glucose monitor (CGM) has evolved far beyond its original purpose as a diabetes management tool. Recently, the FDA cleared the first over-the-counter CGM intended for anyone 18 years and older who does not use insulin, including those without diabetes who want to better understand how diet and exercise impact blood sugar levels. This landmark approval has opened new frontiers in personalized medicine, where metabolic insights drive precision health interventions.
Medical Device Contract Research Organizations(CROs) have become an integral part of the healthcare industry. This article will provide an in-depth look into the world of Medical Device CROs, their offerings, and why they are crucial in device studies.
The complex and dynamic nature of infectious diseases necessitates the need for efficient and effective therapeutic interventions. This has led to an escalating demand for seasoned Clinical Research Organizations (CROs) that specialize in infectious diseases. These CROs play a pivotal role in the successful design and execution of clinical trials aimed at finding impactful treatments and vaccines for various infectious diseases. This article aims to provide a comprehensive guide to identifying the top infectious disease CROs, focusing on their capability to cover vaccines, therapeutics, diagnostics, and their ability to quickly set up studies and recruit quickly due to the dynamic nature of infectious diseases.
Explore the critical role of Good Clinical Practice (GCP) in clinical studies, highlighting how it ensures compliance and enhances the quality of research.
Discover how optimizing clinical data management services can significantly enhance research outcomes.
Explore the intricacies of parallel group design in clinical research with our comprehensive guide.
Discover the essential GCP clinical guidelines that ensure compliance and promote best practices in clinical research.
Discover proven strategies to enhance clinical trial recruitment, ensuring higher participation rates and successful outcomes.
Explore the critical role of Phase IV studies in ensuring drug safety post-approval.
Explore how Electronic Data Capture (EDC) systems are transforming clinical trials by enhancing data management and boosting efficiency.
Discover the essential best practices and innovative strategies for optimizing clinical trial site management.
Discover the crucial role of pivotal trials in clinical research, exploring how these definitive studies influence drug approval and shape the future of medical treatments..
Explore how real-time monitoring is revolutionizing clinical trials by boosting accuracy and efficiency.
Explore the latest best practices and groundbreaking innovations in safety monitoring for clinical trials.
Explore how continuous monitoring is revolutionizing clinical trials by boosting safety and efficacy.
Discover the top 5 CROs to watch for in 2025 and why they stand out.
Discover the essential best practices and innovative strategies for optimizing clinical data management.
Discover the leading clinical data management software solutions set to revolutionize healthcare in 2025.
Unlock the secrets to obtaining FDA approval with this comprehensive step-by-step guide.
Unlock the complexities of database lock in clinical trials with our comprehensive guide.
Delve into the world of early phase clinical trials with this comprehensive guide, exploring their significance, processes, and impact on medical advancements.
Discover the essentials of Good Clinical Practice (GCP) in research with this comprehensive guide.
Discover the leading electronic data capture systems that are revolutionizing data management.