Aloe Vera CVs

Meeting, Montreal, QC, May 26, 2011.

“GMP Identity Requirements: Which Tools and Technologies are Scientifically Valid?” at SupplySide East, Secaucus, NJ, May 3, 2011.

“An Industry Perspective on Botanical Ingredient Standardization,” presented to the Marketed Health Products Directorate, Health Canada, Ottawa, ON, March 25, 2011.

“An Industry Perspective on Botanical Extract Issues and Standardization,” presented to the Natural Health Products Directorate, Health Canada, Ottawa, ON, March 24, 2011.

China Pharmacopoeia Delegation, U.S. Department of Commerce Workshop, Washington, DC, Dec 15, 2010.

“An Overview of GMP Botanical Identity Testing,” at the AOAC Dietary Supplements Task Force and Community Meeting, Orlando, FL, September 26, 2010.

“Herbal Medicine: Issues in Quality, Safety, and Efficacy,” for HRB 632, Tai Sophia Institute for the Healing Arts, Laurel, MD, July 25, 2010.

“Presentation 2: Identity Testing,” for AHPA Vendor Qualification Teleseminar, June 8, 2010.

50 th Anniversary Meeting of the American Society of Pharmacognosy, Poster Presentation “ AHPA’s 2006 – 2007 Tonnage Survey of Select North American Wild-Harvested Plants ”, Honolulu, HI, June 27-July 1, 2009.

NIH Office of Dietary Supplements, Panel Member Presentation at 3 rd Annual Dietary Supplement Research Practicum, Washington, DC, June 3, 2009.

“ Simple Authentication Methods for Herbal Ingredient Integrity in the face of EMA ” at FDA Public Meeting on Economically Motivated Adulteration (EMA) College Park, MD, May 1, 2009.

“AHPA’s Tonnage Survey of Select North American Wild-Harvested Plants, 2006–2007 : Preliminary Results (and Heavy Metal Limits)” at the 6 th Annual Natural Health Product Research Conference and Tradeshow of Canada, Vancouver, Canada, February 19, 2009.

“Heavy Metals in Dietary Supplements,” Interactive General Session, USP Annual Scientific Meeting, Public Discourse – Quality Standards, Kansas City, MO, September 25, 2008.

“Bringing a Supplement to Market,” NIH Office of Dietary Supplements Practicum 2008, Bethesda, MD, June 10, 2008.

“U.S. Regulation of Dietary Supplements: An Overview, also the Application of the SIDI™ Protocol,” Herbal International Summit and Expo on Medicinal, Aromatic Products and Spices Associated Chambers of Commerce and Industry, New Delhi, India, April 5, 2008. “Simple Authentication Methods for Herbal Ingredient Integrity” and “Ensuring the Integrity of Botanical Raw Materials: Application of the Standardized Information on Dietary Ingredients (SIDI™) Protocol,” 5 th Annual NHP Research Conference & Trade Show, Toronto, Ontario, March 27-28, 2008.

“Phytomedicine and Other Botanical Standardization Achievements” for the Georgetown University Survey Course of Conventional and Alternative Medicine, Washington, DC, October 25, 2007.

“Standardization of Botanical Ingredients: A Select Scientific and Regulatory Overview,” Regulations for Nutraceuticals by Intertec-Pira, Washington, DC, October 18, 2007.

“Botanical Standards: Approaches to Characterizing Consistency” in Clinical Pharmacognosy: Contribution of Pharmacognosy to Clinical Trials of Botanicals and Dietary Supplements, Satellite Program at the 48 th Annual Meeting of the American Society of Pharmacognosy, Portland, ME, July 14, 2007.

“Botanical Sciences: Fields of Interlocking Inquiry”, Speaker, Dietary Supplement Education Alliance (DSEA)