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Certara Software

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Phoenix™ PK/PD Platform
Certara's Phoenix™ platform, used by 6000 researchers and 11 global regulatory agencies, is the most comprehensive and widely-used software for pharmacokinetic, pharmacodynamic, and toxicokinetic modeling and simulation.
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Simcyp™ PBPK Simulator
The Simcyp Simulator is the leading physiologically based pharmacokinetics (PBPK) platform for determining first-in-human dosing, optimizing clinical study design, evaluating new drug formulations, setting the dose in untested populations, performing virtual bioequivalence analyses, and predicting drug interactions.
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Pinnacle 21 Enterprise
P21 is a unified cloud suite to streamline the design, build, and submission of clinical trial data, as well as ensure the quality, integrity, and compliance of your data.
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Certara Integral Repository
Certara Integral™ is a single, validated, 21 CFR Part 11 compliant data repository that streamlines clinical pharmacology workflow. with secure and pre-validated technology
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D360™ Scientific Informatics
The D360™ platform, used by over 6,000 discovery scientists for small molecule and biologics research, provides self-service data access and integrated analysis solution.
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Pirana Modeling Workbench
Pirana is a flexible, extendible pharmacometrics workbench that provides structure, tools, and a graphical user interface to facilitate creating models and performing simulations.
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With GlobalSubmit™ eCTD submissions management software, you’ll provide your regulatory team the tools they need to efficiently publish, validate, and review your eCTD submissions.
coauthor all software
CoAuthor provides a solution for regulatory writers that combines generative AI and smart authoring tools to accelerate the creation of regulatory documents.
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SEND Explorer®
SEND Explorer® is a validated, web-based application that addresses data challenges faced by nonclinical scientists by providing advanced viewing, data summarization, and visualization capabilities.
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A.I. powered software CODEX is revolutionizing how clinical trial data can be approached, enabling clinical investigators, trial managers and coordinators to gain new value from internal and external data.
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BaseCase™ engages Market Access, Medical Affairs, Advocacy & Patient Engagement, and Commercial Sales and Marketing stakeholders with interactive, tailored, real time data driven content across the product lifecycle.
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Certara.AI allows you to solve data silo problems while improving analytics capabilities that drive productivity and accelerated data discovery across life science R&D.
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Market Access Radar
Market Access Radar (MAR) is a pharma market access database and repository of more than 8 years with daily delivery of the most up-to-date Market-Access (MA) related news and reports, hand-picked by experts in reimbursement.
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Trial Simulator
Certara’s Trial Simulator leverages existing knowledge for a drug under study with simulation. Users can find answers to critical questions to increase your probability of meeting study endpoints.
Phoenix PK/PD Platform version 8.4

Our Phoenix™ platform is the leading PK/PD modeling and simulation software used worldwide for non-compartmental analysis, population PK, and IVIVC.

With more than 13,000 users including researchers at biopharmaceutical companies, academic institutions, and global regulatory agencies, including the FDA, EMA, and PMDA, Phoenix features a user-friendly interface and built-in visualization and reporting tools to get the outputs you need.

Our last release includes open source plotting, upgrades to Reporter and Phoenix NLME, and more.

Download Version 8.4
Phoenix PK/PD Platform version 8.4
Reach Your Professional Development Goals
Reach Your Professional Development Goals

Certara University provides on-demand and on-site courses.   Our programs are designed for novice and advanced users in the area of pharmacokinetic (PK) and pharmacodynamics (PD) and are taught using Certara software including the industry-standard software Phoenix WinNonlin™.

Learn More
On-Demand Video: PK Submit CDISC Technology

PK Submit automates the time consuming, error-prone and complex task of creating CDISC domains as part of the pharmacokinetic (PK) deliverable for regulatory submissions. It allows you to automatically create a complete electronic regulatory submission-ready package within minutes during the normal process of setting up and executing a non-compartmental analysis (NCA).

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On-Demand Video: PK Submit CDISC Technology

How can we help you?

Contact us today to discuss how we can accelerate your program.