Phase one
Initiation Phase
Establish NDA for confidential discussions
Define project scope, goals, timeline, and data availability
RES submits project proposal
The initiation phase focuses on understanding the client’s request and defining the project scope, deliverables, budget, and timeline. We also conduct a preliminary analysis of the biology and available data to guide the modeling approach.
Phase two
Execution Phase
Develop detailed description of the biological system
Build model integrating biological knowledge and data
Calibrate and refine the model through testing and validation
Create case studies to demonstrate model insights
The execution phase builds confidence in the model through scientific analysis. We review literature and internal data, identify key assumptions, perform sanity checks, and calibrate the model to accurately represent the biological system.
Phase three
Final Phase
Deliver project and regulatory report
The final phase focuses on generating actionable insights from the model. Results may include first-in-human dose predictions, affinity requirements, PK attributes, optimal dosing strategies, and efficacy versus toxicity analysis. These findings are compiled into a comprehensive report suitable for internal decision-making or regulatory submission.
If you have further questions, please reach out via our Contact page.
What exactly does RES do, and how can you help me?
How do I work with RES? What are the first steps?
How much does a project cost and how long will it take?
What does "RES" stand for?