Welcome to our clients and website visitors from outside the U.S...

The Next Phase® Consultancy, Inc. is your gateway to the U.S. marketplace.

If your company is developing products and technologies for the life sciences industries, we can help it enter its NEXT PHASE. We specialize in medical devices and systems, as well as drug delivery and in vitro diagnostic systems used in combination with biotechnology or pharmaceutical product.

You will benefit from:

Nearly 15 years of experience in the life sciences industries and over 20 years of experience in market research, business development and regulatory affairs.
Our own expertise, helping you to...
- understand the market you've targeted:
  - assess the marketplace
  - determine what your end users and customers want from your product
  - learn about your competition:
    - get an easy-to-use overview of your product's competition
    - analyze your product's competition in-depth
- understand your product’s chance for market success
  - assess your product’s marketability
  - receive an objective assessment of your product's or technology's value
  - screen and acquire or divest new technologies
- design and develop your product technology
  - define and document its design based on user needs
  - analyze its design for potential risks
  - engineer your product considering human use factors
- market your product:
  - craft a plan for:
    - marketing
    - promotion
  - create marketing and sales tools
- plan for your business’ future:
  - define your business direction
  - prepare a compelling and convincing business plan for funding
  - create a plan to guide the development and growth of your business
  - target potential partners based on their core competencies
  - arrange partnership agreements and programs
Expertise of our internationally renowned expert associates - through team effort with our associates we can now help you to achieve your regulatory and clinical research goals…
- receive regulatory guidance:
  - understand your options for regulatory approval pathways
  - develop a global and/or U.S.-based regulatory plan
  - prepare and manage your regulatory submissions
  - locate an authorized representative in the U.S.
  - achieve product qualification and validation
- perform pre-clinical and clinical research:
  - understand your research options
  - plan pre-clinical studies and clinical trials
  - perform pre-clinicals studies and clinical trials
Our understanding of a wide variety of markets and technologies
Customized, professionally and discretely managed programs
Solutions that fit your budget and schedule

Hear what our valued clients outside the U.S. have to say about The Next Phase...

We invite you to contact us to learn more about what we can do for you.

Ready for growth... Ready for The Next Phase

Last modified: October 1, 2008

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