Vermont HHP Webinar

November 10, 2026

Complimentary Webinar – Vermont HHP

What’s Next for Vermont’s Groundbreaking Household Hazardous Products Law?
November 10, 2026

Speakers:

· Andriana Kontovrakis, Director of EPR Solutions, Reverse Logistics Group

· Denise Diorio McVeigh, EPR Services and Stakeholder Engagement Manager, Reverse Logistics Group

The Vermont Agency of Natural Resources (ANR) recently published a draft collection plan for implementation of the first-in-the-nation Household Hazardous Product (HHP) Extended Producer Responsibility (EPR) law, tackling end-of-life management for household hazardous waste. The draft plan is the first preview of what practical next steps may be required of obligated manufacturers.

ANR is running the HHP program itself after no industry-led organization stepped in to serve as a producer responsibility organization (PRO). The law’s scope is broad and there is no trade group that represents all, or even most, of the covered products.

Reverse Logistics Group (RLG) is providing critical program implementation support. RLG has been contracted by ANR to support manufacturer outreach and education regarding registration requirements, covered product reporting, and billing.

Hear from RLG on what issues are top of mind for the agency, RLG’s role and how it differs from a traditional PRO setup, what manufacturers can expect to see in 2027, and how to best provide input and get involved with shaping implementation of this groundbreaking law.

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2026 Annual Meeting

December 6, 2026 - December 9, 2026

HCPA’s Annual Meeting is your gateway to growing your expertise, building meaningful connections, and shaping the future of the industry. Join colleagues from across the household and commercial products supply chain in Fort Lauderdale, Florida.

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Beyond LD50 Webinar

January 20, 2027

Title: Beyond LD50: Non-Animal Approaches for Acute Toxicity Testing and Classification

Time: 1:00 – 2:00 pm ET

As regulatory agencies and industry move toward reduced animal testing, new scientific approaches are emerging to support acute toxicity evaluation. This webinar will explore the latest non-animal methods, including in vitro systems, computational models, integrated approaches to testing and assessment (IATA), and defined approaches for acute hazard identification. Case studies will illustrate how these tools can be used to support classification, labeling, and safety assessments while improving human relevance and scientific confidence.

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2027 VOC Webinar Series

January 27, 2027 - March 10, 2027

January 27 | February 10 | February 24 | March 10  - 1:00 – 2:30 pm  ET

Four-Session Webinar Series Rate 
Member: $100 per webinar | $300 for the bundle  
Nonmember: $200 per webinar | $500 for the bundle 

Due to the webinar being recorded for later viewing, substitutions will not be accepted. 

For those unable to attend, the webinar will be recorded and made available via email to registered participants. 

A Practical Guide to Compliance 

Join HCPA for a four-part webinar series to help companies navigate the evolving VOC regulatory landscape and apply that knowledge to their products and business practices. Led by HCPA experts, this practical series will provide the regulatory background, compliance considerations, and tools companies need to evaluate VOC requirements, understand their obligations, and work effectively with business partners throughout the supply chain. 

 Across the webinar series, programming will: 

  • Provide a comprehensive overview of federal, state, and international VOC regulations and their application to consumer, commercial, institutional, and industrial products. 

  • Explain key definitions, requirements, and compliance considerations companies need to understand when evaluating regulated products. 

  • Help manufacturers and marketers work effectively with distributors, retailers, and other supply chain partners to support compliance. 

Part 1: January 27, 2027 – 1:00 – 2:30 pm ET  
Consumer Product VOC Regulations Overview 

Part 2: February 10, 2027 – 1:00 – 2:30 pm ET 
Regulated Consumer Product Categories & Limits 

Part 3: February 24, 2027 – 1:00 – 2:30 pm ET 
How to Determine VOC Compliance 

Part 4: March 10, 2027 – 1:00 – 2:30 pm ET 
Global Requirements, Photochemical Reactivity, and What’s Next 

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CPSC eFiling in Practice: Webinar

February 3, 2027

1:00 - 2:00 pm ET

Due to the webinar being recorded for later viewing, substitutions will not be accepted.

For those unable to attend, the webinar will be recorded and made available via email to registered participants.

Description

On July 8, 2026, importers of regulated consumer products were required to begin electronically filing certificate of compliance data with U.S. Customs and Border Protection (CBP) under the U.S. Consumer Product Safety Commission's (CPSC) revised certificate rule (16 CFR part 1110). The requirement expanded on January 8, 2027, to include products entered for consumption or warehousing from foreign trade zones (FTZs).

With several months of implementation underway, this webinar will explore early enforcement trends, common compliance challenges, and lessons learned. Speakers will discuss how CPSC and CBP are implementing the requirements, common filing errors that can lead to shipment holds, examinations, and delays, and early experiences following the January FTZ deadline.

Designed for manufacturers, importers, and sellers of products subject to CPSC regulations, this webinar will provide practical insight for companies across the household and commercial products industry, including aerosol, air care, cleaning, and floor care products. 

The webinar will include an opportunity for audience questions.

What You Will Learn

  • Early Enforcement Trends: How CPSC and CBP are implementing eFiling requirements, including the impact of missing or incomplete certificate data on entry risk assessments, holds, and examinations. 
  • Common Filing Errors: Frequent compliance issues, including incomplete certificate data, incorrect use of Disclaim codes, and confusion between testing and certificate exemption.
  • Filing Methods and Access: Key considerations when choosing between the Full PGA Message Set and the Reference PGA Message Set (CPSC Product Registry), including managing broker and laboratory access. 
  • General Certificates of Conformity: Requirements for non-children's products, including reasonable testing programs and identifying applicable regulations. 
  • FTZ Compliance: Early experiences and compliance challenges following the January 8, 2027, implementation deadline. 
  • Compliance Best Practices: Practical strategies for recordkeeping, certificate maintenance, and responding to CPSC or CBP requests. 

Speakers

Antonia Stamenova-Dancheva, Counsel, Keller and Heckman LLP

Kyle Wilson, Managing Scientist, Exponent

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Pesticide Labeling Webinar

April 7, 2027

Description: Pesticide labels are governed by a complex framework of federal statutes, regulations, and extensive EPA guidance. However, distinguishing legally binding requirements from recommendations and interpretive guidance is not always straightforward. Understanding how these sources interact is essential for developing compliant labels, navigating regulatory review, and anticipating changes that may affect product registrations.

This webinar will provide a practical overview of the pesticide labeling framework, beginning with the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the labeling requirements outlined in 40 CFR Part 156. Presenters, Michael Boucher and Lisa Amadio, will explain how these requirements are supplemented and interpreted through EPA resources, including the Label Review Manual and Pesticide Registration Notices (PR Notices), and clarify the role each plays in labeling decisions.

Building on this foundation, the webinar will explore emerging regulatory and procedural developments that pesticide registrants should be monitoring. Topics will include changes to label notification procedures, evolving bilingual labeling requirements, and the EPA’s movement toward structured digital labels.

Attendees will gain a clearer understanding of the current regulatory landscape, the implications of these developments for labeling practices, and how to prepare for upcoming changes. Whether responsible for pesticide registrations, label development, or regulatory compliance, participants will leave better equipped to interpret EPA labeling expectations, identify relevant regulatory resources, and navigate an evolving pesticide labeling environment.

Speaker(s):

· Lisa Amadio, Principal, Regulatory Consultant, Ramboll

· Michael Boucher, Partner, Steptoe, LLP

Due to the webinar being recorded for later viewing, substitutions will not be accepted.

For those unable to attend, the webinar will be recorded and made available via email to registered participants.

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