From Data to Decisions.
Your Partner in Quantitative Pharmacology & Modeling.
Development Strategy
Tailor-made modeling strategies to inform your decisions and de-risk your drug development program.
Modeling Solutions
Innovative, agency-endorsed solutions to develop robust predictive models and optimize every stage of drug development.
Regulatory Support
PhinC brings decisive regulatory value to your submission dossier through robust and validated modeling approaches.
Adopt the MIDD strategy and get a head start on your development.
The principle of MIDD is based on an integrated quantitative approach, implemented early in development to generate powerful predictive models, inform strategic decision-making, and secure the progression of the candidate through Phase III.
Modeling solutions for every phase of drug development.
From discovery through to clinical and regulatory phases, PhinC provides expertise in quantitative pharmacology to support decision-making throughout development.
Lead Optimization
Speed up identification of the best targets and candidates.
PhinC helps you rationally prioritize molecules with the greatest therapeutic potential.
Preclinical
Anticipate human translation from the very first data.
PhinC helps you reduce risk and secure your clinical starting dose.
Phase I
Secure the first administration in humans.
PhinC helps you control dose escalation and optimize the design of early studies.
Phase II
Accelerate clinical proof-of-concept.
Optimize the dose-exposure-response relationship and select the right dose.
Phase III
Confirm your large-scale dosing strategy.
PhinC helps you to anticipate variability and reinforce the robustness of your results.
Latest from PhinC.

MIDD and FDA: What Biotechs need to know about ICH M15
The ICH M15 guidance introduces a harmonized framework that allows these models to be formally recognized as “MIDD evidence” by regulatory authorities such as the FDA.

New Publication : Developing a PBPK model for ADC (Oncology)
A first-in-class PBPK model for CLDN18.2-targeted ADCs using PK-Sim® and MoBi®. Read and discover the full article!

10 good reasons to use modeling and simulation
Modeling expertise is an essential cornerstone for a robust and optimal drug development strategy.
Key figures.
+1,000
+300
90 %
+60
They trust us.
“The positive opinion of EMA about Acoziborole, a single dose treatment of the deadly human African trypanosomiasis (HAT) represents a major step forward. Our collaboration with PhinC was instrumental to the success of the project. They supported the program through population PK modeling to characterize drug exposure in HAT patients and quantify variability. This work helped identify intrinsic and extrinsic factors influencing pharmacokinetics. In addition, they conducted concentration-response analyses to support cardiac safety evaluation Their flexibility and expertise enabled us to obtain the right information at the right time to meet regulatory requirements.”
“Simulations Plus has formed a strong relationship with PhinC as we work together to drive increased adoption of physiologically-based pharmacokinetic (PBPK) modeling to support pharmaceutical research and development. Their talented team of scientists have become proficient users of our GastroPlus™ software platform, and we are confident that the services they provide to clients are valuable and greatly impact R&D productivity.”
“Crossject and PhinC have been collaborating for several years on popPK and PBPK modeling activities. The decision to work with PhinC was based on the team expertise in pharmacokinetics and modeling within drug development, and their aptitude to react and to collaborate within a biotech context. Moreover their approach is based on the client listening and project understanding in order to propose the most adequate proposal to the request. Our relationship is very pleasant, efficient and fruitful for both the scientific and project outputs.”