Translational Sciences
Starting your drug or medical device development program correctly is as important as starting quickly and efficiently. Aptiv Solutions can help guide your development programs from inception through to proof of concept and on to marketing.
Our experienced clinical trials team provides a wide range of consulting services for biologics and small molecules including:
Clinical Transitional Science Expertise
- Program design, planning & leadership
- Target product profile development and strategy
- Scientific advisory boards including key opinion leader recommendations
- Risk analysis and contingency plans
- Program planning including timeline and budget management
- Chemistry, Manufacturing and Controls (CMC)
- Preclinical Discovery and Development
- Clinical First-In-Human, Proof of Principle (PoP), Proof of Concept (PoC)
- Product Life-Cycle GxP compliance
- Due diligence & support for funding negotiations
