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This event will be conducted virtually via Zoom.
The "TOP 10" Funding Opportunities from the K4-DealRoom.com site are pre-screened and invited to the monthly Screening Meeting. Deal Flow Silo Chairs, Due Diligence Fellows, Members, and Invited Guests interested in the K4 "Entry to Exit" investment process convene to screen the companies invited to present here to reach the finalists for our Monthly Forum Meetings. K4-MA Members may request remote access attendance.
This Investor Showcase will amplify the voices, innovations, and investment potential of women-led early-stage companies. Designed to go beyond a traditional pitch event, this gathering serves as a catalyst for action—bringing together investors, entrepreneurs, and thought leaders to address the systemic barriers that continue to limit access to capital for women founders.
This event will be conducted virtually via Zoom
This event will be held for our five Mid-Atlantic Chapters including New York, New Jersey, Philadelphia, DC Metro and Pittsburgh.
Eckert Seamans
Liberty Place, 50 S. 16th Street, 22nd Floor, Philadelphia, PA 19102
Keiretsu Forum Philadelphia members and guests are invited to join us at our Host Sponsor, Eckert Seamans, for our Hybrid Forum meeting showcasing 4 exciting companies in the Life Sciences and Technology Silos.
The Due Diligence Training Workshop will be hosted by Keiretsu Forum Mid-Atlantic, South-East & Texas and will be presented by Area President, Howard Lubert.
3650 Lenox Rd - 2 Alliance Center NE Atlanta 30326
We will meet on 16th floor in the Magnolia R
Keiretsu Forum Atlanta members and guests are invited to join us at our Host Sponsor, Warren Averett, to kick off our first Atlanta based Hybrid Forum meeting showcasing 4 exciting companies in the Life Sciences and Technology Silos.
This event will be conducted virtually via Zoom
This event will be held for our South-East & Texas Regions.
Gain a deeper understanding of regulatory readiness and its critical role in life sciences investments at this focused seminar. Focused predominantly on the particular requirements related to medical and wellness devices, the session will clarify US FDA regulatory pathways and their intersection with intellectual property and business law.