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Model-informed Drug Development
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Early Development IND Enabling Services
Drug Development and Regulatory Strategy
Model-based Meta Analysis
Pharmacometrics
Quantitative Systems Pharmacology
Quantitative Systems Toxicology and Safety
Simcyp Physiologically-based Pharmacokinetic Modeling
Virtual Bioequivalence
Phoenix™ PK/PD Software
Phoenix PKPD Platform
Phoenix WinNonlin
Phoenix NLME
Phoenix IVIVC Toolkit
PK Submit
Pirana Modeling Workbench
Trial Simulator
Simcyp Mechanistic Software
Quantitative Systems Pharmacology
Quantitative Systems Toxicology and Safety
Simcyp Biologics
The Simcyp Consortium
Simcyp PBPK Simulator
Simcyp Pediatrics Simulator
Featured Product
Pediatric Practice
Data and Informatics
CODEx and Clinical Trial Outcomes Databases
D360 Scientific Informatics Platform
Integral Data Repository
Pinnacle 21 Regulatory/CDISC Compliance Software
Featured Product
Pinnacle 21 Enterprise Software
Regulatory and Access
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Scientific and Medical Communications and Publications
Safety and Pharmacovigilance
Regulatory Consulting and Regulatory Affairs
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Regulatory Operations
Transparency and Disclosure
Regulatory Technology
GlobalSubmit eCTD Submissions Software
Pinnacle 21 Regulatory/CDISC Compliance Software
Synchrogenix Writer
Evidence, Value and Access
BaseCase Value Communication Software
Decision Analytics and Modeling
Health Economics Outcomes Research
Health Outcomes Performance Estimator (HOPE)
Market Access and Pricing
Real World Evidence
US and EU Payer Engagement
US Managed Markets
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FDA’s Digital Transformation: The Future of Technology and How to Prepare
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Simcyp: 20 Years of Innovation
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Biohaven achieves FDA approval with Nurtec™
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Pinnacle 21 Awarded FDA Contract for 5 Years for Software and Services
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