Pharmacometrics: Support Early Decision-Making
Pharmacometrics: Support Early Decision-Making
Quantitative Insights to Inform Key Development Decisions
Start Strong: Implement Pharmacometrics Early-On
The decisions drug developers make early in the development process are critical because they impact the success or failure of the drug later on. Incorporating pharmacometrics methods early in development helps quantify interactions between drugs and patients, optimizing drug development.
Global Leaders in Pharmacometrics, with a Proven Record of Success
120+
Pharmacometrics consultants over 5 continents
15+
Dedicated PKPD programmers
70+
Clinical pharmacologists, Early drug development, DMPK, CMC, and toxicology experts
800+
Pharmacometrics projects completed in the last 4 years
Pharmacometrics Services for Early Drug Development
We provide a comprehensive spectrum of decision-making support and filing support, based on quantitative analysis methodologies.
- Development of Pharmacometrics Strategy/Project Plan
- Modeling & Simulation Analysis Plans
- Population pharmacokinetic (PopPK) analysis
- Biomarker PK-PD Analysis
- Disease Progression Modeling
- Translational PK-PD Analysis (animal to man)
- Exposure-Response Analysis of Efficacy or Safety
- Cardiovascular Safety Analyses (QTc)
- Model-based Meta Analysis
- Clinical Trial Simulations
Choose Certara: World’s Most Experienced Pharmacometrics Team
With over 120+ pharmacometricians, the Certara Pharmacometrics team designs and implements model-informed drug development (MIDD) strategies for all types of drug development programs, regardless of therapeutic area, drug modality, and development phase.
Fit-for-Purpose
Our experts are skilled at navigating the complexities of each project by creating fit-for-purpose analysis approaches, aimed at addressing the key development questions. At Certara, we value innovation, and leverage strong science, deep expertise, and strategic thinking to overcome our partners’ unique challenges.
Integrated Solutions
As a part of Certara’s Drug Development Solutions family which includes a wide range of drug development service offerings, the team is uniquely positioned to help clients put the results of pharmacometrics analyses in the context of their development strategy and achieve optimal impact on decision-making. With access to CMC, DMPK, Toxicology, and Regulatory Services, every project has access to end-to-end support.
Meet the Experts
Rik de Greef
Senior Vice President, Global Lead, Quantitative Science Services
Stephen Duffull
Senior Scientific Advisor, Quantitative Science Services
Matt Zierhut
Vice President, MBMA Capability Lead
JF Marier
Senior Vice President, Canada Region Lead, Quantitative Science Services
Adekemi Taylor
Vice President, QSS-US-1 Region Lead, Quantitative Science Services
Mirjam Trame
Vice President, QSS-US-2 Region Lead, Quantitative Science Services
Amy Cheung
Vice President, Europe/APAC Region Lead, Quantitative Science
Paul Diderichsen
Vice President, Europe/Africa Region Lead, Quantitative Science Services