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Certara's Better Drug Development Process

The drug development process is long and expensive with more failures than successes.

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How we help our clients

Integrated Drug Development

We tailor clinical pharmacology, pharmacometrics, pharmacokinetic and pharmacodynamic (PK/PD) analysis, and regulatory strategies to get to proof of concept faster, choose the right dose, and reduce clinical trial size or avoid certain trials altogether.

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We accelerate regulatory submissions and approvals with customized regulatory submission strategy, communications and operations, powered by our proprietary artificial intelligence technology and supported by the GlobalSubmit™ eCTD platform.

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We optimize value with decision analytics and modeling, value and access consulting, and real world data solutions, powered by our HOPE™ Bayesian modeling engine and communicated via our BaseCase™ platform.

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Latest from Certara

Webinar

Fostering Pediatric Oncology Drug Development

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Download Phoenix™ v 8.3

Blog

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Case Study

Optimizing phase 3 study design

Article

Go to war with the army you have: a cocktail can fight COVID-19

Publication

Salvaging CNS Clinical Trials Halted Due to COVID‐19

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Our people are our success. Teamwork and our individual differences, experiences, and capabilities are essential not only to delivering on our customer commitments but also to fostering our collaborative culture and world-class reputation.

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We help to empower our partners to make informed decisions by using our expertise and experience in quantitative clinical pharmacology and pharmacometrics.

– Yuan Xiong, PhD Director, Integrated Drug Development

Success isn’t just measured financially at Certara. It is measured in terms of the submissions we have authored, the speed with which we publish documents to regulators, and the technology we deploy to accelerate access to new health technologies. It’s such a pleasure to be part of this ensemble of amazing talent at Certara. I learn new things every day from talented colleagues and clients alike.

– Justin Edge President, Regulatory Science and Evidence & Access

Here at Certara I have access to key experts, and there is great sharing of knowledge and collective team spirit. We are surrounded by great leaders who are still doing science and inspiring work. Every day we make a difference by pushing the boundaries of science forward for our clients and eventually the patients.

– Eva Gil Berglund, PhD Senior Director, Regulatory Strategy