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Archives -- Research & Development
R&D -- Presentations
Does An Orphan Have the Right to More Than One Parent?”  Food, Drug,
Cosmetic and Medical Device Law Digest, New York State Bar Association, Food,
Drug and Cosmetic Law Section, January 1992.
R&D -- Articles
Get to the Clinic on Time.  Regulatory/Reimbursement Panel.  The NIH-CAP
Commercialization Training Workshop.  LARTA.org.  November 10, 2014.  Los
[no slides]

Creative Strategies in Dealing With FDA.  PSC Creative Learning Webinar.  July
10, 2013.

Creative Strategies in Dealing with FDA.  Compliance2Go. Webinar.  February
21, 2013.

Get to the Clinic on Time. LARTA NIH-CAP Commercialization Workshop,
November 1, 2011. Los Angeles.

Regulatory Challenges in Executing Global Clinical Studies.  The Conference
Forum’s 2nd Annual Executing Global Clinical Trials Conference.  September 15,
2011, Philadelphia.

FDA Regulatory Considerations for the Biomedical Start-Up.  Israeli Life
Sciences Fellows Program, Merage Foundation. February 27, 2008, Irvine, CA.

FDA Regulatory Strategies for Fast Growing Companies. LARTA NIH-CAP
Commercialization Training Workshop, October 17, 2007, Marina Del Rey, CA.

FDA Regulatory Considerations in Launching Products.  Women In Technology
International (WITI) San Diego Conference, February 14, 2006, San Diego.

FDA Regulatory Challenges for the Biomedical Start-Up.  NIH-CAP Workshop,
LARTA, October 7, 2005, Newport Beach, CA.
Key Abbreviations
© 2014   Michael A. Swit.  


Contact me @ 760-815-4762
Michael A. Swit