Audrey Hill, Senior Director, Data Management, Advaxis, Inc., explains the keys to clear...
- The Fundamentals Behind Effective Data Management
- We Need to Talk About Race: Lack of Diversity in Clinical Trials is a Public Health Issue
- Sample Tracking Automation: Do I Have Your Consent?
- Industry Viewpoints: The Pivotal Role of Skilled and Experienced Data Managers in Clinical Trials
- General Data Protection Regulation: The Impact on Clinical Trials and Data Subjects
Enriched Evidence Generation: Linking Clinical Data, Registries and Patient-Reported Outcomes to Health Care Utilization
Eric Van Ganse, Manon Belhassen, PELyon, & Francois Gavini, Roche, explain how French national claims data can deliver critical value to clinical trials and patients registries
Expert Insights: Another Failure for BACE1 Drugs Raises Questions about Alzheimer’s Disease Treatments
Alessio Brunello, MSc, Neurology & Ophthalmology Analyst, GlobalData, explores the implications of Janssen’s decision to halt its Alzheimer’s disease clinical trial
Expert Insights: Can FDA Approval of Cimzia for Psoriasis Secure UCB’s Position in the Immuno-dermatology Market?
Vikesh Devlia, MSc, Immunology Analyst, GlobalData, examines the implications of the FDA’s recent approval of UCB’s Cimzia drug
We Need to Talk About Race: Lack of Diversity in Clinical Trials is a Public Health Issue
Lisa Valtierra, Valtierra Consulting, explains why the lack of data representing diverse patients could lead to worse health outcomes
Sample Tracking Automation: Do I Have Your Consent?
Ron Bourque, MedImmune, explains how with informed consent it’s the non-standard processes that govern the collection of the samples
Industry Viewpoints: The Pivotal Role of Skilled and Experienced Data Managers in Clinical Trials
Dr Raphaela Schnurbus, Clinical Solutions Director, OPIS, explains to Henry Kerali why the role of data managers continues to evolve
Using CDISC SDTM, ADaM and SEND for Regulatory Submissions
Kevin Burges, Head of Product Management, Formedix, discusses the role of CDISC standards in regulatory submissions
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