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Case Study
AI is changing how we answer the first question on every trial: can this be done, where and how fast?
TFS HealthScience is implementing AI to deliver feasibility assessments faster. See how AI and human judgement work together to answer every trial’s first question.
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Case Study
How our Medical Writing Team went from Synopsis to Protocol in two months
How the TFS Medical Writing team delivered a clinic-ready protocol in two months, from a single slide deck.
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White paper
FSP vs Full-service CRO: a plain-English guide for German and Swiss Biotech
A plain-English breakdown of FSP vs full-service CRO for DACH biotech, covering local regulatory context and what to look for in a partner.
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White paper
Navigating the Regulatory and Scientific Complexities of Combination Therapy Protocols
Combination therapy trials require clear, compliant protocols to manage complexity and risk. Download our white paper for expert medical writing insights on effective protocol development.
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Webinars
Managing Placebo Risk in Dermatology Trials
Gain practical strategies for managing placebo risk and ensuring credible, compliant dermatology trial results.
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White paper
Rethinking Clinical Operations: A Smarter, Faster Playbook for Trial Success
Learn how results-driven frameworks, integrated digital systems, and innovative strategies are transforming clinical operations.
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Found 195 Results
Page 1 of 22
Article
10 oncology trial readouts to watch for at ASCO 2026
Biomarker-defined populations. Rare cancers. Multi-country designs. As ASCO 2026 approaches, TFS HealthScience outlines the ten oncology trials that matter most and what they mean for sponsors planning their next programme.
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Article
From single-injection vision restoration to gene therapy: what precision ophthalmology means for trial design in 2026
Learn how ARVO 2026 signals a new era of precision ophthalmology, where smarter recruitment, imaging consistency and patient‑centric design demand deep‑tier partnerships like those offered by TFS.
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Article
News
News
Is your ClinicalTrials.gov results submission overdue?
The FDA reminded over 2,200 sponsors to submit overdue ClinicalTrials.gov results. This how TFS Medical Writing team can help.
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Article
The Value of Cross-Functional Expertise in Complex Oncology Clinical Trials
Experienced Oncology CROs with cross-functional expertise strengthen complex oncology clinical trials and accelerates clinical development.
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Article
Top 5 Challenges in Psoriasis Clinical Trials (and How to Overcome Them)
Psoriasis clinical trials face predictable hurdles, from patient recruitment shortfalls to regulatory complexity. This blog explores the five most common challenges and practical strategies sponsors can use to overcome them.
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Article
From Strategy to Patients: Adaptability and Innovation in Trial Design
Explore how adaptability, innovation, and patient focus can help sponsors rethink trial execution, from smarter sourcing models to the role of AI in oncology.
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Article
Navigating Today’s Clinical Trials: Strategies for Sponsors Facing a Shifting Landscape
Explore how sponsors can stay ahead of evolving regulatory demands, tech shifts, and enrollment pressures in today’s complex clinical trial landscape.
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Article
Rare Neurological Disease Trials: Smarter Design with Natural History, External Controls, and Real-World Evidence
Discover how natural history data, external controls, and RWE are reshaping rare neurological disease trials for smarter, regulatory-ready design.
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Article
ICH E6(R3) Is Here. Is Your Trial Ready?
Discover how TFS is helping sponsors prepare for ICH E6(R3) with proactive oversight, modern technologies, and quality-first trial design.
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