Webinar: Strategies for Compliance with the New York Menstrual Products Right to Know Act Tuesday, December 17, 2019 (11am - 12:30pm US/Eastern)

Cost: $150/BAHP Members; $200/Non-Members

The State of New York recently passed The Menstrual Products Right to Know Act, a groundbreaking law requiring the labeling of ingredients in menstrual products on packages. This state law is the first of its kind in the United States and will impact both product manufacturers as well as companies throughout the supply chain.

In this webinar, Mark Duvall, Principal, Beveridge and Diamond, and Jane Wishneff, Executive Director, Center for Baby and Adult Hygiene Products, will provide a background and overview of the law’s requirements and strategies for compliance.

What This Webinar Will Cover:

• An overview of law requirements and what you need to know
• Practical strategies and best practices for compliance
• Insight into policy trends and increased NGO focus on femcare product ingredients

About the Speakers:



Jane Wishneff – Executive Director, Center for Baby and Adult Hygiene Products

Jane Wishneff is Executive Director of The Center for Baby and Adult Hygiene (BAHP), which represents manufacturers of absorbent hygiene products in North America. Jane has fifteen years of association experience working with policymakers and regulators on behalf of BAHP, the International Fragrance Association North America (IFRANA) and the Consumer Specialty Products Association (CSPA) on issues including chemicals management policy, ingredient communications and consumer product safety. Jane is also a licensed attorney in the District of Columbia and Virginia.



Mark Duvall – Principal, Beveridge and Diamond

Mark has more than two decades of experience working in-house at large chemical companies. His focus is product regulation at the federal, state and international levels across a wide range of programs, and occupational safety and health issues. He leads the firm’s Chemicals group and Occupational Safety and Health practice as well as the firm’s FDA practice, having worked on FDA regulation of food and food additives, dietary supplements, drugs, medical devices and cosmetics, and European counterparts. Mark has counseled clients on the regulation of consumer products by the Consumer Product Safety Commission and the Federal Trade Commission. Mark has also worked on green chemistry issues at the federal and state levels, as well as a variety of voluntary programs that affect products.

Registration Fees: These fees are available through 12/17/2019
Name	Price	Available To
Webinar Registration	$200.00	Everyone