January 4, 2015



We understand that, as a start-up, you’re laser-focused on developing your product – which leaves little time to do the myriad other things that must get done. 

We do those “other things” for you:  For IND-enabling study planning, we bring to the table the expertise you need to achieve clinical-stage quickly and efficiently, by building a comprehensive, regulatory-compliant, executable plan – and driving plan execution. We can help you create both a regulatory and clinical development strategy, plan and manage clinical research studies, communicate with FDA (including filings), conduct market research & analysis, help you develop your pitch deck, and more! 

We work with you to create and manage an operating structure that works for you and your team — one that’s organized, flexible, and that frees up your time to focus on things only you can do.

We’ll keep you on track and facilitate an information exchange that will help you meet your goals.

We’re here for you when you need nimble support with experienced helping hands.

Our Promises

   Easy to work with
    Robust processes & flat operating structure make partnering with us easy for you.

   Tailored to your needs
    Excellent understanding of your space and challenges. We quickly tailor services
    that meet your needs and deliver timely, high-quality results.

   Advice & management you can trust
    Our core team and network of experts average 20+ years of experience.

Therapeutic Categories

  • Neurosciences
  • Infectious Disease & Vaccines
  • Oncology, Immuno-oncology, Cell Therapy
  • Immuno-Inflammation
  • Cardiovascular & Hepatocellular
  • CBD-Based Therapies
  • Schedule II Therapies
  • Ophthalmology
  • Rare Disease
  • Biosimilars
  • Generics