Replies to post #75089 on Intellicell Biosciences Inc (fka SVFC)

[mave_rick]

The Face of SVFC Could Change Forever

To answer your question Pennyboy,The Time To Complete the IND Once approved by the FDA , is not a Definitive time but rather a Range. I suspect that it will be as less than 3 months, But Dr. Victor has repeatedly said that he plans on and is excited about doing several other IND's as well. Conducting these INDs takes time and Resources.

I Like the Underlying "Thought" level at which Intellicell is operating and Practicing for the Future in starting the very first IND getting the FDA involved and projecting several other INDs. They are simply doing what they can and must in a Systematic ORDER to Effect a Turnaround.

The PPS reflects a "Different Class of Trader/Investor" BUT as the Company continues to Raise the Awareness Level of its Technology, and all things they are Engaged in to include but not limited to the Current IND ,future INDs, The Andrews Licensing agreement as a Revenue Generator, the International Patent, and as the General National Environment for Stem Cell research continues to evolve and change with ultimately BIG PHARMA and Hospitals, Doctors, and Insurance Companies becoming more INCLUSIVE of this kind of Treatment and Therapy and Technology, the FACE Of SVFC could Potentially, and I Believe WILL CHANGE FOREVER.

THINK BIG IMO

IMO ONLY

[cazual]

SVFC $$$$

Can pre-IND meetings reduce time to market? Yes, time can be reduced by the following:

Identifying and avoiding unnecessary studies
Ensuring that necessary studies are designed to provide useful information
Gaining FDA support for a proposed strategy
Potentially minimizing potential for clinical hold
Providing opportunity for creative exchange of ideas
Obtaining regulatory insight
Minimizing costs
Clearly defining endpoints and goals of the development program
Allowing early interactions/negotiations with FDA

http://www.fda.gov/Drugs/DevelopmentApprovalprocess/SmallBusinessAssistance/ucm069906.htm