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Biomarker analysis
Biomarker Testing
With laboratory services that span the development lifecycle and industry-leading scientists with extensive drug development experience, IQVIA Laboratories can help you simplify and align co-development strategies to speed development and increase probability of regulatory and commercial success.
Our services include
Related Insights
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Managing Informed Consent Samples from Clinical Trials
A set of best practices for the definition, tracking and management of allowable use attributes associated with samples collected in protocol based clinical trials
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Biorepository and Specimen Management
Your biological specimens are irreplaceable assets – trust them with a proven partner
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ADME Services
Accelerating your drug discovery, preclinical and clinical programs
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IQVIA Laboratories Central Laboratory Services
Central laboratory solutions supporting clinical trials around the world
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Helping you master your lab data
Improved oversight with your lab data now in full view
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NASH and Liver Disease Capabilities
Nonalcoholic Fatty Liver Diseases & Non-alcoholic Steatohepatitis (NAFLD & NASH)
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How COVID-19 Changed Clinical Trial Dynamics and Environment
Precision Medicine World Conference 2021 Virtual Presentation
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Pediatric Initiative
Optimizing small blood volumes to prevent canceled tests in clinical trials for pediatric patients
Vaccine Laboratory Services
Test Menu
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SARS-CoV-2 Vaccine Induced Antibody Profiles
Presented at World Vaccine Congress 2021
Related Services
- Anatomic Pathology Laboratory Services
- Bioanalytical Services
- ADME / DMPK Services
- Biomarker Services
- Biotech Laboratory Solutions
- Central Laboratory Services
- Clinical Genomics Laboratory Services
- Companion Diagnostics (CDx)
- COVID-19 Clinical Trial Solutions
- Flow Cytometry Assay Development
- Translational Science and Innovations Laboratory Services (TSAIL)
- Vaccine Laboratory Services