At Certara, behind every successful pharmacometric analysis is a skilled and multidisciplinary team that bridges science, data, and strategy. Experts in clinical pharmacology, biostatistics, and modeling work collaboratively to generate insights that guide decision-making and regulatory communication. Our expertise ensures that population analyses and exposure-response studies are meticulously designed and executed, addressing the complexities of patient variability and therapeutic outcomes. By leveraging the collective knowledge of the team, organizations can facilitate smoother regulatory submission pathways and optimize drug development efforts.
Pharmacometrics for Regulatory Submission Support
Pharmacometrics services for regulatory submissions
モデリング&シミュレーションサービス
Learn more about pharmacometrics for regulatory submission support
The role of an experienced team in pharmacometrics
Tailored submission strategies
Our fit-for-purpose pharmacometrics solutions are designed to address your specific development questions and provide clear support for dose regimens, safety, and efficacy in regulatory submissions.
Streamline regulatory submissions
Certara’s pharmacometrics experts deliver robust analysis to support drug labeling and meet regulatory expectations, ensuring compliance through precise PopPK, PKPD, and exposure-response modeling.
End-to-end regulatory support
With access to clinical pharmacology, regulatory strategy, and additional services, Certara ensures your pharmacometrics analyses are seamlessly integrated into your regulatory package for optimal impact.
Pharmacometrics expertise for regulatory success
サターラのサービス
Pharmacometrics strategy & planning
- Development of strategy and project plans
- モデリング&シミュレーション解析計画
- Frontloading analyses (early unblinding)
Data analysis & reporting
- PopPK and PKPD modeling
- Exposure-response analysis (efficacy/safety)
- Simulations to support dose regimen justification
- Pharmacometrics reports
Regulatory submission support
- Electronic submission package
- Clinical summaries and labeling components
- Addressing questions during regulatory review
サターラの専門家
お問合せはこちら
Our team is ready to assist you with tailored pharmacometrics strategies that optimize drug development and ensure regulatory compliance. Let us help you navigate the complexities of regulatory submissions with confidence.
お問い合わせはこちら
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FAQs
ファーマコメトリクスとは何か?
Pharmacometrics involves the modeling and simulation of pharmacokinetics and pharmacodynamics to inform drug development and regulatory decisions.
サターラは承認申請をどのようにサポートしていますか?
Certara provides a full spectrum of pharmacometric services, including PopPK, PKPD, and exposure-response analyses, along with expert regulatory guidance.
What sets Certara apart in pharmacometrics?
Our global team, innovative strategies, and integrated approach ensure tailored, impactful solutions for every project.