Learn more about Lindus Health from our blog page. Our posts cover an array of topics from clinical developments to diversity.
Traditional clinical trials rarely reflect how consumers actually use OTC and self-care products. Real-world evidence (RWE) fills this gap by capturing adherence, satisfaction, and safety data at scale to build credible, regulator-ready claims.
For sponsors developing rapid infectious disease diagnostics, the landscape is shifting fast. Traditional lab tests take hours or days, but rapid diagnostics deliver results in minutes. This shift creates a significant challenge: clinical trial strategies designed for slow, centralized tests won’t work for fast, decentralized ones.
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.
For medical device companies looking to grow globally, expanding into both the US and EU often feels like the logical next step. But many teams quickly learn that what works in one region doesn’t always translate to the other. Despite some similarities, the US and EU operate within different regulatory and commercial frameworks.
GLP-1 receptor agonists are quickly becoming versatile treatments with proven effectiveness in cardiovascular disease, chronic kidney disease, sleep apnea, and Alzheimer’s Disease. Early clinical data suggest they may also help in neurodegeneration, osteoarthritis, and other inflammatory conditions, making this drug class a potential game-changer in metabolic medicine, where specialized CRO support is critical for navigating complex clinical development.
Discover the essential best practices and cutting-edge tools for optimizing clinical trial data management.
Explore the critical role of Phase IV clinical studies in drug development, uncovering how they ensure long-term safety and efficacy of medications post-approval.
Explore the intricate world of clinical research with our essential guide.
Explore the transformative landscape of clinical research services as innovation unlocks new possibilities.
Dive into the fascinating world of clinical research with our comprehensive guide, exploring its various types and their pivotal roles in advancing medical science and improving patient care.
Navigate the intricate world of drug approval with our comprehensive guide to the NDA New Drug Application process.
Dive into the fascinating world of medical research with our comprehensive guide.
Explore the intricacies of parallel study design with our comprehensive guide.
Navigate the complexities of Good Clinical Practice (GCP) regulations with our comprehensive guide.
Discover how EDC clinical studies are transforming data management in clinical trials, enhancing accuracy, efficiency, and compliance.
Explore the fundamentals of parallel group studies in clinical research, a key design that compares different treatment groups to assess efficacy and safety.
Delve into the world of clinical studies with our comprehensive guide.
Dive into the world of clinical research with this insightful article that unravels its meaning and underscores its critical importance in advancing medical science and improving patient care.
Delve into the world of Phase 4 clinical trials with this insightful article, exploring their significance in post-marketing surveillance, patient safety, and the ongoing development of medical treatments.
Unlock the full potential of your data strategy with our comprehensive guide to electronic data collection.
Discover innovative and proven strategies to enhance patient recruitment in clinical trials.
Explore the intricate journey of drug development with our comprehensive guide.
Discover proven strategies for conducting an Investigational Device Exemption (IDE) study with our comprehensive guide.
Discover the fundamentals of clinical trials, their significance in medical research, and how they contribute to advancements in healthcare.
Unlock the full potential of the EDC Database with our comprehensive guide.