This is the FVTC Venture Center’s most interactive, impactful, business improvement process we’ve ever offered. We’re helping small businesses, non-profits and corporations design business models built for the future.

Behind every successful e-seed entrepreneur is a trusted mentor and guide. Now, we’re bringing the program that launched hundreds of new businesses right to you.

E-seed for Direct Sellers - based on the Direct Selling Entrepreneur Program Curriculum, a joint project of the Direct Selling Education Foundation (DSEF) and National Association for Community College Entrepreneurship (NACCE) - is designed to equip direct sellers with small business management and entrepreneurial skills to operate more successful direct selling businesses.

-Do you need to identify high-growth, emerging, or shrinking markets?

-Are you looking at benchmarks on competition?

-Do you need market intelligence to improve your profit making decisions?

The FREE Explore: Growing Your Direct Sales Business seminar provides an initial look inside what it takes to launch a successful, home-based, business.

3 critical things you MUST do to launch and sustain a business

A weekly meet-up with a distinctly social twist where people can expect to find their entrepreneurial compatriots.

FACE-2-FACE with Martha Stewart, Founder, Martha Stewart Living Omnimedia. Come discover inspiring stories and business advice from well-known executives across America each month.

This FDA warning letter closeout program will discuss how to successfully complete warning letter close out program which will help firm to obtain a closeout letter from FDA.

The manufacturing requirements for early stage clinical trials are designed to assure adequate quality of the investigational product being tested without the excessive regulatory burden of full-scale GMP manufacturing. This workshop will present the current regulations, guidance documents and regulatory strategies available for manufacturing an early development stage product for Phase I and first-in-man clinical trials. Also discussed will be logistical issues with managing the supply of an early stage investigational product, and requirements for stability testing, storage and shipping, labeling, and documentations. Perspectives for different classes of products will be presented using case studies.