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Our Early Phase Clinical Development solutions provide expert support at every stage, from Candidate Selection through Phase 1.
Strategic guidance and end-to-end support to navigate global regulatory pathways, ensuring efficient and compliant drug development from preclinical stages through
Our experienced pharmacometrics services team helps quantify drug-patient interactions, optimize development & regulatory choices.
Choose Certara's Quantitative Systems Pharmacology (QSP) consulting services to enhance drug development with computational modeling and experimental data.
Analysis and strategies with the main objective of ensuring a successful drug development program.
Global consulting team applying PBPK modeling to all stages in drug development.
Advanced biostatistics consulting and CDISC-compliant SDTM & ADaM datasets
Our regulatory writing services offer expertly crafted, high-quality documents for drug development, ensuring compliance and timely submissions.
Discover Certara's comprehensive Real-World Evidence Services. We provide innovative RWE solutions for pharma, empowering regulatory, market access, and clinical strategies.
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