PATIENT DATA REPORTING FEATURED ARTICLES
PATIENT DATA REPORTING WHITE PAPERS & ARTICLES
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Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.
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Clinical trial protocols are the blueprints of research, yet they remain locked in static, text-based documents that must be manually reinterpreted across each clinical system.
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As the global reliance on algorithms and artificial intelligence (AI) continues to grow, the importance of data quality and completeness has become a critical concern.
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Examine challenges and solutions in epilepsy trials, including electronic diaries, placebo response training, and integrated cognitive assessments, transforming research approaches.
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Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.
PATIENT DATA REPORTING APPLICATIONS & STUDIES
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Commercializing Rare Disease Treatment With Near Real-Time Alerts5/16/2025
How did Quest help a leading pharmaceutical company overcome the data latency challenges associated with traditional EHR when recruiting eligible patients for a rare blood disorder drug?
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Understanding Real-World Patient Characterization And Safety Outcomes Of DEXTENZA5/8/2025
In this study, we can derive confirmation of DEXTENZA’s favorable safety profile across a broader surgical spectrum.
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EHR-To-EDC Success In A Complex, Adaptive Platform Trial4/17/2025
I-SPY 2, one of the longest-running adaptive platform trials in oncology, is revolutionizing breast cancer research through a dynamic, data-driven approach to evaluating novel therapies.
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Pioneering The End-To-End Decentralized Trial Experience4/16/2025
Explore a collaboration between a top 20 pharmaceutical company and Medidata that highlights the potential of DCTs to transform trial execution, offering a replicable model for future research.
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Digital Outcome Measures Approved As Primary Endpoint In Cardiopulmonary Study4/15/2025
Discover how a clinical development program was saved using objective, continuous digital outcome measures.
PATIENT DATA REPORTING SOLUTIONS
- eSource: The Evolution Of Clinical Trial Data Capture
- Modernizing Clinical Research Through Digital Transformation
- Electronic Informed Consent For Clinical Research
- Flexible Solutions To Facilitate Comprehension And Compliance
- eSource Element
- Drug Accountability And Returns Management
- ePRO And Castor Connect
- Rave RTSM: Optimize The Setup And Execution Of Repeat Visits
- Selecting And Evaluating An eRegulatory Solution
- Industry-First eTMF AI Reduces Risk Of Document Misfiles And Metadata Errors
VIDEOS
NEWS
- Australia Delivers Certainty For US Biotechs In 2025: Avance Clinical Offers Fast Start-Up, Regulatory Predictability, And R&D Rebates
- Reduce Complexity For Oncology Sites, Sponsors, Patients, And Caregivers
- Meet With Avance Clinical At ASCO 2025 In Chicago
- Avance Clinical Honored With Frost & Sullivan's 2025 Global Customer Value Leadership Award
- Novotech Welcomes New Investment From GIC, Temasek, And Existing Investor TPG To Accelerate Global Growth
- Novotech Report Reveals Global Surge In Infectious Disease Trials As Industry Nears 2,000 Studies Since 2020
- Novotech Identifies Strategic Opportunities In Idiopathic Pulmonary Fibrosis Trials With Release Of Global Market Insights
- Crucial Data Solutions Sets Another Industry Benchmark: TrialKit Now Available As A Native macOS App
- Avance Clinical To Showcase Asia-Pacific Clinical Trial Expertise At BIO Korea 2025
- Novotech Expands South Korean Presence With New Hospital Trial Site Deal
- Novotech Named Best Contract Research Organization In Australia At Asia-Pacific Biopharma Excellence Awards 2025
- Novotech Report Reveals Growth In siRNA Research
- Sikich Recognized As NetSuite Winter 2025 Alliance Partner Spotlight Award In Biotech and Biopharma
- Crucial Data Solutions Launches Industry-First Subscription Model To Modernize Clinical Trial Contracting and Pricing
- Rally For Rare 2025: How Scout Delivered In Just 3 Days
- Global Reach For Biotechs: Avance Clinical Secures MOUs With Four Premier Taiwanese Trial Sites
- Avance Clinical Expands In Asia With Taipei Office To Accelerate Biotech Clinical Trials
- Novotech Partners With Kyungpook National University Hospital To Strengthen Clinical Trial Capabilities In South Korea
- Medable Is The First Digital Trial Vendor To Achieve Landmark CNIL Approval
- Simbec-Orion And Avance Clinical Consolidates Partnership With Memorandum Of Understanding
- ActiGraph And Hyfe Announce Availability Of New Digital Health Tool For Cough Monitoring
- Novotech Releases Comprehensive Report On Oncolytic Virus Therapy
- Novotech Releases Report On Current State Of Triple-Negative Breast Cancer Clinical Trials
- Comparing Eye Exams In Mobile Settings To In-Office Exams
- ActiGraph Accelerates Clinical Trial Modernization With Transformational Acquisition Of Biofourmis Life Science Business
- Avance Clinical Leads As The CRO Of Choice For Early Phase Clinical Trials In Australia – Announced At Biotech Showcase 2025
- Novotech Releases Report On Global Parkinson's Disease Clinical Trial Landscape
- Novotech Named A Fierce CRO Award Winner In The Excellence In Clinical Trial Management And Global Operations Categories
- Novotech Publishes Report On The Global COVID-19 Clinical Trial Landscape
- OpenClinica Named Top Contender In Electronic Data Capture (EDC) Platforms By Everest Group