Once the agreement is signed, we initiate the project immediately and begin execution according to the defined plan.
Talk to us about your regulatory, safety, or R&D needs in respiratory toxicology.
In the meeting we will discuss your compounds, products, or regulatory challenges, explore how ALIsens® fits into your development or compliance strategy, and give you the opportunity to speak directly with our CEO and CSO for a focused technical discussion.
We review your needs internally and define the project scope, including scientific milestones, expected outcomes, deliverables, and timelines.
We prepare and send a clear technical and commercial proposal explaining how your challenges will be addressed, including methodology, costs, and execution plan.
Once the agreement is signed, we initiate the project immediately and begin execution according to the defined plan.
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