TOP 10 FROM THE EDITOR
1.
How CVS, Walgreens, And Walmart Will Improve Clinical Trial Recruitment
2.
What Astellas Has Learned About Decentralized Trials
3.
How BMS Uses AI To Improve Study Design And Reduce Costs
4.
AI's Potential To Improve Clinical Operations, Trial Matching
5.
AstraZeneca Hopes To Advance Oncology RWE
6.
The Future Of TransCelerate: Clinical Trial Modernization
7.
How Is The Role Of Clinical Data Manager Changing?
8.
Boehringer Ingelheim Implements One Medicine Technology Platform
9.
Takeda Takes A Strategic Approach To TMF
10.
How One Pharma Company Is Embracing Digital Technologies
TOP 10 GUEST COLUMNS
FDA Releases Draft Guidance On Decentralized Clinical Trials
By Sean Hilscher, MBA, MA, Greenleaf Health
4 Pitfalls Of Poor-Performing Clinical Trial Teams — And How To Prevent Them
By Monica Roy
Reflecting On The Syneos Health Acquisition: The Due Diligence Imperative
By Darshan Kulkarni, Pharm.D., MS, Esq., Kulkarni Law Firm, and host of Darshan Talks podcast
3 Reasons People Don’t Enroll In Clinical Trials — And How To Overcome Them
By Adrelia Allen, Merck
Why Do So Many Alzheimer’s Clinical Trials Fail?
By RJ Tesi, MD, INmune Bio
The 5 Vs Of Collecting Clinical Data
By Steve Chartier, Society for Clinical Data Management, Patrick Nadolny, Sanofi, and Richard Young, Society for Clinical Data Management
FDA Issues New Guidance On Dose Optimization For Oncology Therapies
By Marjorie Zettler, Ph.D., MPH, Regor Pharmaceuticals, Inc.
Save Time And Money By Using AI To Compare CRO Proposals
By Audrey Rossow
Designing Quality Into Your TMF: ICH E6(R3) And Advancing Trial Efficiency
By Ken Keefer, MBA, PMP, Keefer Consulting Inc.
Where Are All The Arabs? And How A U.S. Census Change Could Improve Clinical Trial Diversity
By Hadi Danawi, Ph.D., Arab Board for Clinical Research
TOP 10 INDUSTRY INSIGHTS
The (True) Patient Journey
By Scout Clinical
Risk Mitigation In Direct-To-Patient Clinical Trials
By Nicole Gray, Catalent
Complete Guide To FDA Inspection Readiness
By Advarra
3 Key Functions Your eTMF Needs To Meet New EMA Regulations
By Robert Toal, IQVIA Technologies
Roche Cuts Feasibility Process By 36%
By Cognizant
eSource: The Evolution Of Clinical Trial Data Capture, Monitoring, And Management
By Medidata, a Dassault Systemes company
Risk-Based Approach To Monitoring Of Clinical Investigations
By Lyn Agostinelli And John Sikora, Halloran Consulting
No More Excuses! Small Biotechs Report Growing Dissatisfaction With CROs
By Harbor Clinical
The Value Of Tokenizing Clinical Development Data
By Zelta
5 Ways FDORA Will Impact Clinical Research Sponsors
By Elligo Health Research
TOP 10 SOLUTIONS
The IQVIA Investigator Site Portal
IQVIA Technologies
10 Questions For Choosing A Mobile Research Nursing Provider
PCM Trials
Selecting And Evaluating An eRegulatory Solution
Florence Healthcare
A Day In The Life Of A Clinical Research Coordinator
OpenClinica
Patient Recruitment And Site Selection
Novotech
GxP Auditing: Ensuring Quality And Compliance
Harbor Clinical
Proper Data Management Across All Areas And Phases
inSeption Group
Cut Study Start-Up Times By Up To 50% With eCOA
Medidata, a Dassault Systemes company
SIP Simplifies Collaboration Between Sites And Sponsors
Cognizant
Trial Recruitment At Warp Speed
Citeline
