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EPA’s New Hazardous Waste Pharmaceutical Rule: What to Expect and How to Comply

EPA’s New Hazardous Waste Pharmaceutical Rule: What to Expect and How to Comply

Product Code: YNWA111418

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EPA’s New Hazardous Waste Pharmaceutical Rule: What to Expect and How to Comply

Live Webinar: Wednesday November 14, 2018

2:00 p.m. to 3:00 p.m. Eastern / 11:00 a.m. to 12:00 p.m. Pacific


WEBINAR SNAPSHOT: Understand how the new hazardous waste pharmaceutical rule will impact your business operations and what you’ll need to do to comply and avoid fines.



ALERT: Changes to the 2015 Management Standards for Hazardous Waste Pharmaceuticals are coming in October 2018.

The EPA issued its proposed Management Standards for Hazardous Waste Pharmaceuticals in September 2015, under new subpart P of 40 CFR Part 266 for the management of hazardous waste pharmaceuticals by health care facilities and pharmaceutical reverse distributors. The complexity of the proposed rule has been a factor in it taking over two years for the EPA to finalize its provisions.

One of the biggest changes in the proposed rule, scheduled to become final in October 2018, is that health care facilities, such as pharmacies, hospitals, physicians’ offices, and long-term care facilities, will be subject to simpler, less stringent hazardous waste regulations while pharmaceutical reverse distributors are likely to be subject to much heavier regulation than in the past.

As proposed, the rule also distinguished between creditable and non-creditable hazardous waste pharmaceuticals, with a non-creditable hazardous waste pharmaceutical being a pharmaceutical that is notexpected to be eligible for manufacturer’s credit. 

Join us on November 14 for an in-dept and informative webinar led by attorneys Greg Blount and Karlie Webb. They will carefully assess the rule requirements and discuss the implications of the final rule on both health care facilities and pharmaceutical reverse distributors. 

Attending this webinar will:

  • Eliminate the confusion associated with the numerous new requirements of the final hazardous waste pharmaceuticals rule
  • Provide tips to enable you to comply with the new rule
  • Clarify how the new rule will impact your business 
  • Enhance your understanding of the implications for retailers and reverse distributors
  • Inform you of the reactions to the final rule from industry professionals|
  • Decrease the likelihood of making the common errors involved in any new set of rules

About Your Presenters:

Greg BlountGreg Blount, Esq.
Partner
Troutman Sanders LLP 

Greg Blount has broad experience representing clients in matters related to environmental law and policy for over 35 years, including related civil litigation and enforcement issues in state and federal courts. His experience includes work for retail chains, including pharmacies, on retail and pharmaceutical hazardous waste issues, as well as serving as national environmental counsel for a Fortune Top 10 company during extensive negotiations in California, Connecticut, Florida, Illinois, Kansas, and New Jersey.

Mr. Blount and his colleagues continue to remain very active in hazardous waste compliance and policy work at federal and state levels, particularly in California.

Karlie WebbKarlie Webb, Esq.
Counsel
Troutman Sanders LLP 

Karlie Webb has a national practice, focusing on representing corporations, industry groups, and individuals in all aspects of environmental law, including regulatory compliance, rulemaking, and permitting, particularly under RCRA, CERCLA, and EPCRA. She also defends federal and state environmental enforcement actions and advises on facility-wide environmental compliance issues.

Ms. Webb commonly represents chain retailers, including grocers and pharmacies, among others, on retail and pharmaceutical hazardous waste issues, including advising on compliance with applicable federal and state regulatory schemes, permitting, and extensive negotiations with state environmental regulators to settle compliance claims.

Have a specific question related to the topic of this audio conference? Post it here and get an answer during the event, time permitting, or in a follow-up e-mail from the audio conference presenter. This is only available to audio conference registrants.

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