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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.
The clinical research ecosystem is a complex network of various stakeholders, including sponsors, investigators, patients, regulators, and a host of service providers known as clinical research vendors. These vendors play a critical role in ensuring the successful execution of clinical trials, and their expertise ranges from full-service delivery of clinical trials (CROs), patient recruitment, to mobile nursing and phlebotomy. This article aims to delve into the different categories of clinical research vendors, highlighting top players in each category.
Clinical research services (CRS) are the backbone of medical progression and discovery, providing essential support to clinical studies on groundbreaking treatments, novel drugs, and innovative therapies. Clinical research services are typically responsibilities delegated to Contract Research Organizations (CROs). These services are pivotal in facilitating the journey of medical advancements from the laboratory to the patient's bedside. This article delves into the in-depth panorama of clinical research services, shedding light on various facets of this indispensable domain.
Discover the transformative power of Clinical Trial Management Systems (CTMS) in optimizing clinical trials.
Discover how electronic data capture is revolutionizing clinical trials by boosting accuracy and efficiency.
Unlock the essentials of Good Clinical Practice (GCP) in clinical research with our comprehensive guide.
Discover effective strategies to enhance patient enrollment in clinical trials, ensuring timely recruitment and diverse participation.
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.