
ABOUT TFS HEALTHSCIENCE
TFS HealthScience is a full-service, global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance innovative treatments and improve patient outcomes. With operations across 40 countries, TFS and its strategic partners provide tailored strategic resourcing solutions and clinical development services in specialized therapeutic areas, including dermatology, internal medicine, neuroscience, oncology, and ophthalmology. Dedicated to empowering partners and enriching lives, TFS offers flexible solutions that combine global reach with the agility and responsiveness of a mid-sized CRO.
FEATURED ARTICLES
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This playbook provides a concise yet comprehensive roadmap for navigating Europe’s multifaceted regulatory environment when conducting gene therapy trials involving GMOs and CDx.
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In today’s clinical development environment, DCT technologies are not optional innovations; they are essential drivers of more resilient, efficient, and patient-focused trials.
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By leveraging real-time data and predictive tools, sponsors and CROs can address the increasing complexity of trials, accelerate therapeutic development, and proactively manage risks.
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The Huntington’s disease (HD) landscape is undergoing rapid transformation driven by breakthroughs in gene-targeted therapies, small-molecule modulators, regenerative medicine, and digital innovation.
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Explore how AI is redefining the development pipeline for neurodegenerative diseases (NDDs), offering a path forward in the quest for effective, disease-modifying treatments.
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Explore how strategic resourcing, particularly through FSP models, empowers biotech sponsors to overcome common hurdles transitioning when from preclinical research to first-in-human (FIH) trials.
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To optimize clinical development, the pharmaceutical industry is increasingly adopting innovative outsourcing strategies with CROs.
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Real-world evidence (RWE) is transforming clinical trials by enabling the use of external control arms (ECAs), which serve as an alternative to traditional randomized control groups.
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Learn seven of the critical factors for choosing an oncology-focused CRO that enable sponsors to identify partners aligning with their clinical research objectives.
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Learn how to employ data-driven insights, artificial intelligence, and decentralized clinical trials to accelerate drug development and address the intricate challenges of neuroscience research.
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The 2025 American Academy of Dermatology (AAD) Annual Meeting underscored pivotal advancements in dermatology drug development, highlighting the essential role of innovative dermatology CROs.
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Immunotherapy is revolutionizing oncology, enhancing patient outcomes through targeted treatments. This evolving landscape includes checkpoint inhibitors, and personalized medicine, shaping the future of cancer care.
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Overcoming barriers to gene therapy development requires continued innovation in manufacturing processes, harmonized regulatory approaches, and outcome-based pricing models.
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The CTR and CTIS represent a paradigm shift in European clinical research, fostering a more efficient and transparent trial environment.
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The release of the ICH E6(R3) Good Clinical Practice guideline in January 2025 marks a shift in clinical research, with significant implications for CROs, trial design, and quality management.
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Learn about the key criteria that sponsors should evaluate when selecting a partner for your IO trials to help them improve efficiency, and accelerate the development of life-saving cancer treatments.
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AI and data-driven innovations are transforming dermatology clinical trials by enhancing efficiency, data accuracy, and patient access.
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Recent breakthroughs are signaling a promising shift in the landscape of Epidermolysis bullosa (EB) care from focusing on pain management to a growing commitment to curative strategies.
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Advancements in genetic therapy are revolutionizing the treatment of neurological diseases, with promising results from preclinical studies leading to clinical trials focused on safety and efficacy.
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Explore the critical role of study coordinators, emphasizing their expertise, strategic contributions, and the value they add to clinical research.
CONTACT INFORMATION
TFS HealthScience
2530 Meridian Parkway Suite 300
Durham, NC 27713
UNITED STATES
Phone: +46 (0)46 280 18 00
Contact: info@tfscro.com
FEATURED PRODUCTS
TFS HEALTHSCIENCE CASE STUDIES
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This time-sensitive Phase 3 trial in dry eye disease required precision project management leveraging strong site relationships, ophthalmology-specific expertise, and data-driven site selection.
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This partnership allowed a leading biopharmaceutical company to navigate the complexities of a Phase IIb study investigating a novel pegylated RNA adapter for geographic atrophy secondary to dry AMD.
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Discover how a tailored, risk-based project management approach was used to overcome the challenges of a complex Phase I/IIa FIH multi-country study of an advanced therapy medicinal product (ATMP).
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A European biotech company collaborated with TFS HealthScience to conduct an early-phase clinical trial focusing on advanced and metastatic solid tumors.
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To address a life-threatening complication of immunotherapy in hematologic malignancies, a U.S. biotech company developed a novel compound.
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Through strategic planning, adaptive trial execution, and proactive collaboration, TFS successfully navigated the complexities of this early-phase oncology study.
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How did a Phase III combination study for neovascular age-related macular degeneration (AMD) overcome study complexities while expanding across 16 countries?
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A strategic partnership enables a U.S. biotech company to address the struggles with their Phase I first-in-human oncology trial.
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Effective site selection is critical for the success of DMD gene therapy trials. This study details innovative methodologies employed to streamline and improve site identification.