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ALL CONTENT CLINICAL LEADER

  • When Survival Comes First, Trials Come Last
  • Why Are We So Afraid To Pay Research Participants?
  • J&J Taps Tau-Based Diagnostics To Improve Alzheimer's Disease Trial Design And Enrollment
  • Transforming Cardiac Monitoring In Biopharma With 6-Lead And 12-Lead Devices
  • Transformative Cardiac Solutions
  • CDISC's New 360i Helps Move Trial Design From Manual To Modern
  • 5 Cs For Responding To FDA-483s — Strategies For Effective Compliance And Resolution
  • Introducing Arcinova, A Quotient Sciences Company
  • Age Restrictions In Clinical Trials Unjustly Harm Adults With Childhood Cancer
  • The 3 FDA Oncology Approvals That Will Have The Biggest Impact In 2025
  • The FDA's New Guidance May Be Shaking Up Biotech
  • Designed To Help Sites Increase Clinical Trial Capacity
  • 5 Best Practices For Improving AI Literacy In A GxP Environment
  • AI Data Security: The 83% Compliance Gap Facing Pharmaceutical Companies
  • All Of Us Need To Be Rooting For The FDA
  • Why Is Hep C Still On The Rise? And What Atea Is Doing About It
  • DCT Benefits Are Proven, Yet Progress Is Slow
  • All You Need To Know About 505(b)(2), But Were Afraid To Ask
  • Trials Without Borders: A Webinar Series From Clinical Leader And FlexPoint Bio
  • New Purpose-Built Facility For Large-Scale Sterile Fill/Finish Operations
  • Advanced Drug Delivery And Drug Device Combination Product Solutions
  • Paving The Way For Sites To Use Their Own Tech
  • What Sponsors Must Know About Digital Systems And AI Compliance
  • Regulatory Advantages Of Clinical Trials In Canada Versus Australia
  • More Personalized, Precision Medicine Needed In Psychiatry Clinical Trials
  • Health Economics And Outcomes Research (HEOR) Explained
  • Drug Price Controls: What Are The Unintended Consequences To Innovation?
  • November 9-12: ISPOR Europe 2025: Powering Value And Access Through Patient-Centered Collaboration
  • September 28-30: ISPOR Real-World Evidence Summit 2025: Through The Lens Of Asia Pacific
  • September 10-11: Communicating HEOR For Maximum Impact, Influence, And Understanding
  • Quotient Sciences Announces Formation Of Scientific Advisory Board
  • Meet Avance Clinical At 2025 KoNECT-MOHW-MFDS International Conference (KIC)
  • Meet Avance Clinical At BIO Asia-Taiwan 2025
  • In-Vivo CAR Therapies — Global Research And Development Landscape
  • Analytics–Powered Approach To Patient Recruitment Strategy
  • Off-Script FDA: How Smart Teams Pivot, Escalate, And Progress
  • 4 Centralized Comparator Sourcing Models To Fortify Supply Chains
  • How To Avoid Hazards And Map A Safer, Smarter Path For AI, Part 2
  • How To Avoid Hazards And Map A Safer, Smarter Path For AI, Part 1
  • Clinical Trials Get A Council For AI Oversight
  • From Protocol To People: Teva's Patient-First Clinical Trials Approach
  • A Guide To Guidelines: How ICH And Others Help Us Conduct Better Trials
  • Streamline Recruitment With Confidence
  • Recruiting High-Performing Sites To Beat Forecasted Trial Start Date
  • A New Approach To Dynamic Clinical Oversight With Centralized Insights
  • RWD, New Technologies Show Potential In Clinical Trial Recruitment
  • Use Case: How Consulting & Analytics Can Guide Clinical Strategy
  • Sickle Cell Cure Within Reach, But At A Steep Cost
  • How An Australia-First Strategy Cut 63% From Our R&D Spend
  • Part Of $1 Billion Investment Strategy, PCI Pharma Services Completes Acquisition Of Ajinomoto Althea, Enhancing U.S. Drug Product Manufacturing For Aseptic Filling Of Prefilled Syringes & Cartridges
  • Suvoda And Greenphire Announce Completion of Merger
  • Imunon Talks Passionate PIs, Endpoint Selection In Frontline Ovarian Cancer Trials
  • Leveraging Real-World Data From The IRIS® Registry
  • Live Biotherapeutic Products: Unique Quality, Manufacturing, And Nonclinical Considerations For Clinical Trial Entry
  • Novotech Showcased In Global Biotech Series For Innovation In Hepatitis B Research
  • Agentic AI And How It's Impacting Clinical Trial Research
  • Powering More Efficient Clinical Development With AI And ML
  • Accelerating CRO Study Deployment At Scale
  • Tufts & PACT Release New DCT Analysis
  • Continuous Cough Monitoring: Addressing Placebo Effects And Data Gaps
  • ActiGraph Is Rebranding As Ametris
  • eSource Purpose Is Not Just To Complete The EDC
  • Dear Pharma, The Creator Economy Is NOT Only For Beauty
  • 2 Challenges In Designing A Clinical Trial Exploring Personalized Elimination Diets
  • Planning Your IND: When And Why To Engage The FDA
  • How We Used Intelligent Automation to Transform Vendor Selection
  • Reframing Clinical Vendor Selection
  • Accurate Diagnosis And Enrollment Criteria Improve Intracerebral Hemorrhage Research
  • Hey, What's The Big Idea? Patient Enrollment Utterly Reimagined, That's What
  • PI's CRAACO Model + AI = Rapid Enrollment
  • Breaking Free From The Acronym Soup: Rethinking The Role Of Technology In Clinical Trials
  • Cutting-Edge Innovation Steals Spotlight On London Biotechnology Show 2025 Exhibition Floor
  • Fortrea Optimizes Site Matching On Retina Clinical Trials
  • Expert Guidance For EU Gene Therapy And Companion Diagnostic Trial Regulations
  • Gilead Art Campaign Captures The PBC Patient Experience, Inspires Patient-Centric Trials
  • Pioneering Cancer Research Meets Unparalleled Veeva Vault Integration
  • Population-Aware Medicine: Mitigating Racial Disparities In Efficacy And Accuracy
  • Rapid Results In A High-Stakes Dry Eye Disease Trial
  • Global Start-Up For Multinational Geographic Atrophy Trial
  • Access EHR Data Easily To Identify Patients
  • Leverage Expertly Curated Data To Make Effective Site Selections
  • Overcome The Burden Of Administrative Tasks To Maintain Compliance
  • Generate Accurate And Meaningful Insights With AI
  • Actionable Insights To Improve Your Operational Performance
  • It's Time To Change How We Engage Research Sites
  • The Effects Of Most Favored Nation Drug Pricing On Clinical Trial Management
  • Navigating FDA Regulatory Changes: Policy Shifts, Deregulation, Restructuring, And Future Oversight
  • Understanding FDA's Draft Guidance: Composition Statements Of Ingredients In Labeling In NDAs And ANDAs
  • How Is RIM Software Transforming Regulatory Compliance?
  • Why CRA Proficiency Needs A Boost From Better Assessment And Training
  • Why Omnichannel Isn't Optional
  • How Do You Look At Patient Retention?
  • Tailor Tactics By Trial Type
  • Don't Underestimate HCP Awareness Campaigns
  • Clinical Research Education Isn't Just For Patients
  • No Stipends, But You Will See A Doctor
  • Manage Exponential Data Growth With Medidata Clinical Data Studio
  • Clinical Data Studio: A Single Data Review Platform Fostering Unification Across Groups
  • Disclosure Management System: Build Or Buy?
  • Completed Clinical Trials Continued To Climb In 2024
  • Data Key In Addressing Patient Recruitment Challenges
  • EMA Guideline On Clinical-Stage ATMPs Comes Into Effect: On The Verge Of Convergence?
  • Single Peptides & Pig Testing: How Longhorn's Developing Its Universal Flu Shot
  • The Moments That Made Us
  • Overview Of Central eSource From CRIO
  • BioMarin Generates Patient Experience Data With Early And Often Engagement
  • How Sponsors Can Drive Success With Central eSource At Investigator Sites
  • Achieve Financial Management Success With Rave CTFM
  • Immunohistochemistry In Precision Medicine: From Biomarker To Clinical Trial Assay
  • 5 Ways To Make Your Investigator Meetings Fun And Functional
  • 25 Tips To Prepare A Clinical Site For FDA Inspection
  • Connecting Manufacturers And Providers To The Services Needed For Full End-To-End Patient And Order Management
  • 2 Ways To Overcome The Challenge Of Developing Neurological Rare Diseases Drugs
  • Hidden Compliance Risks In Start-Up That Could Derail Your Clinical Trial
  • Nanoform Starts Pivotal Human Bioequivalence Studies Of Nanoenzalutamide
  • A Look At Elsa, The FDA's New AI Digital Assistant
  • Precision Project Management In Action
  • J&J Survey Of Oncologists Reveals Challenges With Awareness & Access
  • Leveraging AI To Transform Neurodegenerative Drug Development
  • Optimizing EDC Strategy And Data Collection for a Rare Disease Trial
  • How Compassion Shaped This Pediatric Rare Disease Trial
  • Improving Recruitment Needs More Than Transactional Fixes To Earn Patient Trust
  • Wearables For Optical Cardiovascular Monitoring
  • Deriving Reliable Clinical Outcome Scores From Continuous DHT Data
  • Running A 697-Patient MS Study Through Crisis And Complexity
  • Boosting Recruitment Strategy For Phase III Study In Ulcerative Colitis
  • Effective Recruitment Capabilities And Outstanding Customer Service
  • U.S. Tariffs And Their Tenuous Impact On Clinical Trials
  • Insights From 250+ Regulatory Inspections
  • 6 Tips To Ensure Revenue Integrity And Compliance In Clinical Operations
  • When CRO Selection Went Sideways, Ashvattha Therapeutics Did This To Recover
  • Organizational Assessment For A Large MedTech Company
  • Optimizing Site Activation To Accelerate Clinical Trials
  • Evolving Neurology And Neuroinflammation Therapies And Trials In 2025
  • Everything To Know About Long-Term Data Collection For Cell And Gene Therapy Trials In The EU
  • Nurturing Clinical Site Relationships Drives Trial Success
  • Regeneron Trials Balance Quest For "Scientific Truth" With Patient Impact
  • Radiopharmaceuticals: Navigating FDA Guidance And CMC Considerations
  • Why Perfect Clinical Trial Data Is A Dangerous Myth
  • The Future Of Clinical Trials Is Neurodiverse
  • In The Age Of AI, Data Is Still King
  • Australia Delivers Certainty For US Biotechs In 2025: Avance Clinical Offers Fast Start-Up, Regulatory Predictability, And R&D Rebates
  • RWD's Significance In The Largest FDA-Funded IOL Study Of Pediatric Patients
  • Verana Health: Where Quality Powers Insights
  • Utilizing Curated Data To Boost Your Urology Research And Innovation
  • Make Sense Of Unstructured Data In Neurology, Urology, and Ophthalmology
  • Designing More Representative Trials Through Strategic Planning
  • Quality Insights For Ophthalmology Innovation
  • Providing Rich Quality Data In The Neurology Space
  • Expanding The Role Of External Control Arms
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