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.
he relentless pursuit of medical advancement has led to a surge in the demand for high-quality clinical research. With an ever-growing number of pharmaceutical and biotech companies outsourcing their research and development (R&D) processes, the role of Clinical Research Organizations (CROs) has become indispensable. This article sheds light on the top CROs in the US, highlighting their strengths, core service offerings, and unique features that make them a preferred choice for sponsors.
The global contract research organization (CRO) market is a rapidly evolving industry. It has become increasingly crucial for pharmaceutical, biotech, and medtech industries that rely on these organizations to test, refine, and market their latest drugs and devices. The CRO market is projected to grow at a compound annual growth rate (CAGR) of around 10.7% from 2023 to 2028, reaching an estimated worth of USD 127.3 billion by 2028. This article provides an insightful overview of the top 5 CROs that are currently leading the industry.
Discover innovative and effective strategies for recruiting participants in clinical trials.
Unlock the secrets to a flawless IDE submission with our comprehensive step-by-step guide.
Discover innovative and effective strategies for enhancing patient recruitment in clinical research.
Discover innovative and proven strategies to enhance patient recruitment for clinical trials in this comprehensive article.
Discover how Electronic Data Capture (EDC) is revolutionizing clinical trials by streamlining data collection, enhancing accuracy, and accelerating research timelines.
Explore the essential world of clinical data management in our comprehensive article.
Discover essential strategies for optimizing clinical trial management in our latest article.
Explore the intricate journey of drug development in our comprehensive guide.
Explore the diverse landscape of clinical studies in our comprehensive guide.
Dive into our comprehensive guide on Investigational Device Exemption (IDE) to uncover the essential processes, regulations, and implications for medical device development.
Discover innovative and proven strategies for enhancing clinical trial recruitment in our latest article.
Dive into the world of clinical research with our comprehensive guide! This article unpacks the definition of clinical research and explores essential concepts that drive medical advancements.
Discover everything you need to know about Clinical Trial Management Systems (CTMS) in our comprehensive guide.
Explore the essential principles of Good Clinical Practice (GCP) in our comprehensive overview.
This blog explores key strategies to minimize dropout, including building strong relationships between participants and study staff, implementing flexible study designs to reduce participant burden, and providing personalized mental health support throughout the trial.
This blog offers a comprehensive overview of key strategies to enhance recruitment in ophthalmology clinical trials.
Discover the essential role of Institutional Review Boards (IRBs) in clinical trials.
Discover the crucial role of Institutional Review Boards (IRBs) in research ethics.
Explore the diverse landscape of clinical trials in our comprehensive guide.
This blog explores the design and development considerations for point-of-care (POC) diagnostics, highlighting their potential to improve accessibility, speed, and accuracy in healthcare, while ensuring usability and positive patient outcomes.