Services
At Quantivis, we help biotech and pharma teams integrate quantitative medicine strategy into every stage of drug development aiming to reduce risk, accelerate timelines, and strengthen both regulatory and investment confidence. Our services are designed to deliver and implement strategic insight, provide execution excellence, and build sustainable capability.
We offer the following services:
Model-Informed Drug Discovery & Development (MIDD)
Clinical Pharmacology and Biomarkers
Translational Pharmacology and Human Dose Prediction
Dose Selection, Dose Optimization, and Clinical Trial Design.
Strategy development to de-risk your development plans and find opportunities for acceleration
Strategic Accelerator
Vendor identification, selection, and oversight for pharmacometrics (such as population PK, PKPD, QSP, PBPK and MBMA) and clinical pharmacology services
Interim management and senior leadership support for clinical pharmacology, pharmacometrics, and translational science teams
Senior scientific review of study plans, data analyses, reports, and regulatory documents
Gap Analysis and Due Diligence Support for Teams and Investors
Scale and strengthen your team with senior leadership and/or implementation and execution excellence
Capability Builder
PK/PD fundamentals and advanced translational concepts
Model-Informed Drug Development strategy and application
Translational pharmacology risk assessment
Dose optimization and precision dosing principles
Coaching and mentoring clinical pharmacology, biomarker, and pharmacometrics scientists
Build durable quantitative medicine capability through customized training programs and workshops, including:
Team Developer
Flexible Engagement Models
We recognize that every organization’s needs are unique. Quantivis offers flexible and fit-for-purpose engagement models to meet you where you are.
Choose the model that fits your goals and timeline:
Fractional Support: Embedding senior leadership (clinical and translational pharmacology, pharmacometrics and translational science) to implement and execute strategy without long-term overhead.
Project-Based Consulting: Focused consulting for strategic assessments, due diligence, and/or regulatory milestones (IND, BLA/NDA).
On-Demand Consulting: Scale support up or down as priorities evolve.
Workshops & Training: Custom capability-building programs for teams or entire organizations.
How we work
Quantivis works through a pragmatic, fit-for-purpose approach that is laser- focused on impact. We operate in an agile manner, tailoring quantitative and translational strategies to the specific scientific, clinical, and organizational context of each program. We scale our effort to appropriately match the required outcome.
Our work leverages broad cross-therapeutic experience and deep subject-matter expertise, enabling rapid identification of value-creating quantitative analyses and execution approaches.
We facilitate collaboration with a trusted global network of specialized vendors and domain experts, integrating their capabilities as needed to accelerate delivery, manage risk, and ensure high-quality outcomes without unnecessary complexity.
Why Choose Quantivis?
25 years of leadership in Clinical Pharmacology, MIDD, and Translational Science in global pharmaceutical and biotechnology R&D.
Deep experience across large variety of therapeutic areas, drug modalities and drug development phases
Proven regulatory success across global submissions (INDs, NDAs, BLAs, MAAs)
Trusted leader of high performing teams and advisor to boards, investors, and executive R&D teams
Internationally recognized thought leader in the design and execution of model-informed drug development and quantitative pharmacology
Let’s Work Together
Whether you need strategic guidance, embedded leadership, or capability building, Quantivis is your partner in translating data into knowledge to deliver therapeutic impact.