Starting your drug or medical device development program correctly is as important as starting quickly and efficiently. Aptiv Solutions’ medical device and pharmaceutical development consultants can help guide your development programs from inception through to proof of concept and onto marketing.

Our experienced Translational Sciences team, with staff located in the U.S. and EU, provides a wide range of consulting services for biologics, small molecules, and medical devices including:

Translational Science Consulting Expertise

Program design, planning & leadership for pharmaceuticals and medical devices, including:

  • Target product profile development / medical device development / strategy
  • Scientific advisory boards, including key opinion leader (KOL) recommendations
  • Risk analysis and contingency plans
  • Program planning, including timeline and budget management
  • Chemistry, Manufacturing and Controls (CMC) for biologics and small molecules
  • Preclinical discovery, development, and CRO services
  • Early phase clinical services to support First-In-Human (FIH), Proof of Principle (PoP), Proof of Concept (PoC)
  • Product lifecycle GxP compliance
  • Due diligence & support for funding negotiations