Apr
13

EPA Denies Petition to Revoke Chlorpyrifos Tolerances

EPA recently posted the following article on the Agency’s Pesticide website:

“In this Order, EPA denies a petition requesting that EPA revoke all tolerances for the pesticide chlorpyrifos under section 408(d) of the Federal Food, Drug, and Cosmetic Act and cancel all chlorpyrifos registrations under the Federal Insecticide, Fungicide and Rodenticide Act. The petition was filed in September 2007 by the Pesticide Action Network North America (PANNA) and the Natural Resources Defense Council (NRDC).

***

Order Denying Petition to Revoke All Tolerances for the Pesticide Chlorpyrifos (PDF)(45 pp, 4 MB, March 2017)”

Click here to read the entire article.

Mar
28

Nominations to the Pesticide Program Dialogue Committee Open until April 21, 2017

EPA’s Office of Pesticide Programs posted the following notice on its website:

“EPA’s Office of Pesticide Programs is currently accepting nominations for the Pesticide Program Dialogue Committee (PPDC). A federal advisory committee, PPDC provides advice and recommendations to the EPA on issues associated with pesticide regulatory development and reform initiatives, evolving public policy and program implementation issues, and science issues associated with evaluating and reducing risks from the use of pesticides.

Mar
09

NAS Low Dose Toxicity Project Nearing Completion

The National Academy of Sciences is conducting an EPA-sponsored review that could relate to EPA pesticide toxicity assessments. The title of this NAS project is: Unraveling Low Dose Toxicity: Case Studies of Systematic Review of Evidence.  It has the following “Project Scope”:

Feb
21

TPPC Meets

EPA recently published the following notice on the agency’s pesticides website:

“The Tribal Pesticide Program Council (TPPC) will hold its next semiannual meeting on March 8 and 9, 2017, from 8:30 a.m. to 5:00 p.m. (Eastern Standard Time) in Crystal City, Virginia, at One Potomac Yard, Room S4370/80, and on March 10 from 8:30 to 11:30 a.m. in Room S7100. Tentative agenda topics include a discussion on the status of the pesticides in Indian Country report, a presentation on the FIFRA statute, and discussions on the following:

  • EPA’s draft Bed Bug Outreach Plan for tribes;

Feb
09

Court Rejects Most of NGOs’ ESA Pesticides Claims

The United States Court of Appeals rejected most of the environmentalist NGOs’ claims in the case Center for Biological Diversity v. EPA. The court provided the following summary of its lengthy decision (footnotes omitted”):

“The panel affirmed in part, and reversed in part, the district court’s dismissal of plaintiffs’ claims arising from their citizen suit alleging that the U.S. Environmental Protection Agency violated the Endangered Species Act (“ESA”) when it registered certain pesticide active ingredients and pesticide products without undertaking consultation with the National Marine Fisheries Service and the United States Fish and Wildlife Service (collectively “the Service”).

Jan
19

EPA Publishes Final Applicator Certification Rules

EPA has published final rules updating the existing regulation concerning the certification of applicators of restricted use pesticides in response to public comments received on the proposal and based on stakeholder review of the existing regulation and its implementation since 1974. These final rules are effective March 6, 2017. Click here for EPA’s Federal Register notice of these final rules, which contains more details and relevant links.

Jan
04

CRE Comments on EPA’s Atrazine ECO Risk Assessment

Trending: Track and Trace

CRE filed comments on EPA’s draft Ecological Risk Assessment for atrazine (“ERA”).  CRE’s comments included the following conclusion and recommended EPA actions:

There are no field data–no real-world data–supporting the ERA’s modeled effects. EPA should revise its ERA to be consistent with this fact.

If EPA still believes that some change in the current ecological assessment and regulation of atrazine may be necessary, then EPA should first take the following actions:

1) Validate the ERA models in accordance with the principles discussed above;

2) Develop field data supporting any changes proposed by EPA;

Dec
22

EPA Releases Guidance on a Voluntary Pilot Program to Reduce Animal Testing

On December 20, 2016, EPA published the following press release:

“EPA is announcing the start of a voluntary pilot program to evaluate the usefulness and acceptability of a mathematical tool that estimates the toxicological classification of a chemical, which is used in the Globally Harmonized System of Classification and Labeling of Chemicals (GHS) and which is referred to as the GHS Mixtures Equation. This mathematical tool can be used as an alternative to acute animal oral and inhalation toxicity studies for pesticide formulations. EPA is now providing guidance on how pesticide companies can voluntarily submit data for the GHS Mixtures Equation Pilot Program.

Dec
15

CRE Comments at Glyphosate SAP

On December 14, 2016, the Center for Regulatory Effectiveness commented at EPA’s Science Advisory Panel reviewing EPA’s assessment of the carcinogenic potential of glyphosate. CRE’s comments agree with EPA’s conclusion that glyphosate is not likely to be carcinogenic to humans at doses relevant to human health risk assessment. Any contrary EPA conclusion would violate the Information Quality Act. Click here to read CRE’s oral comments at the SAP meeting.

Nov
17

EPA Reschedules Glyphosate SAP

EPA sent out the following notice:

“The Federal Insecticide, Fungicide, and Rodenticide Act Scientific Advisory Panel (SAP) will meet December 13-16, 2016, to consider and review a set of scientific issues being evaluated by the Environmental Protection Agency (EPA) regarding EPA’s evaluation of the carcinogenic potential of the herbicide glyphosate.  This is the meeting that was rescheduled from October 18-21, 2016.

EPA has published meeting materials in docket EPA-HQ-OPP-2016-0385 at www.regulations.gov, including a glyphosate issue paper with the Agency’s proposed classification that glyphosate is not likely to be carcinogenic to humans at doses relevant for human health risk assessment. The meeting materials, charge, panel members and panel biosketches for this SAP meeting are also posted on the Scientific Advisory Panel website.”

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