Edit, Download, and Sign the Reregistration Eligibility Decision on 1,3-Dichloropropene

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How do I fill this out?

To properly fill out this form, begin by gathering all necessary documents and data related to your pesticide product. Carefully read the instructions included with this RED to ensure you understand the requirements. Be mindful of the deadlines for submission and provide complete and accurate information.

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How to fill out the Reregistration Eligibility Decision on 1,3-Dichloropropene?

  1. 1

    Gather all relevant documents and data.

  2. 2

    Read the instructions carefully.

  3. 3

    Complete the required sections of the form.

  4. 4

    Submit your responses by the due date.

  5. 5

    Retain copies of your submissions for record-keeping.

Who needs the Reregistration Eligibility Decision on 1,3-Dichloropropene?

  1. 1

    Pesticide manufacturers who need to re-register their products.

  2. 2

    Environmental regulators monitoring compliance.

  3. 3

    Agricultural businesses using 1,3-Dichloropropene for crop management.

  4. 4

    Researchers studying the effects of pesticides.

  5. 5

    Legal professionals advising clients on pesticide regulations.

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How do I edit the Reregistration Eligibility Decision on 1,3-Dichloropropene online?

On PrintFriendly, you can easily edit this PDF to make necessary changes. Use our intuitive PDF editor to add or modify text, annotations, and other elements of the document. Simply save your edits and download the updated file for your records.

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What are the instructions for submitting this form?

To submit this form, please send the completed document via email to the Special Review and Reregistration Division representative at karen.jones@epa.gov or fax it to (703) 308-8047. Alternatively, submissions can be mailed to the EPA at 1200 Pennsylvania Ave NW, Washington, DC 20460. Ensure all required responses are included to avoid delays.

What are the important dates for this form in 2024 and 2025?

Important dates for 2024 and 2025 regarding the submission of responses are outlined in the document. Initial responses are due 90 days from receipt, with subsequent responses due after 8 months. It is crucial to adhere to these timelines to ensure compliance.

importantDates

What is the purpose of this form?

The purpose of this form is to ensure that all pesticide products meet the regulatory standards set by the EPA. It allows the agency to assess the human health and environmental risks associated with the active ingredient 1,3-Dichloropropene. Furthermore, the form provides a clear path for manufacturers to follow in order to maintain compliance.

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Tell me about this form and its components and fields line-by-line.

This form contains several components that must be accurately completed for compliance.
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  • 1. Registrant Information: Includes details about the company and contact information.
  • 2. Pesticide Product Details: Specifications regarding the pesticide in question, such as active ingredients and usage.
  • 3. Safety Data: Information on toxicity, environmental impact, and required safety measures.
  • 4. Response Timeline: Sections outlining deadlines for submission of data and responses.

What happens if I fail to submit this form?

Failure to submit this form may lead to enforcement actions, including suspension of product registrations. It is essential to adhere to submission timelines to avoid such penalties. The EPA will take appropriate actions if the responses are not received in the designated time frame.

  • Product Suspension: Delay in submission can result in the suspension of your pesticide products.
  • Legal Consequences: Failure to comply may lead to legal challenges under pesticide regulations.
  • Market Impact: Non-compliance can affect product availability and market access.

How do I know when to use this form?

This form should be used when seeking to re-register pesticide products that contain 1,3-Dichloropropene. It is specifically required after the initial registration period has expired. Use this form to ensure compliance with EPA regulations and to assess the safety of the product.
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  • 1. Re-registration of pesticide: To maintain the legality of pesticide products in the market.
  • 2. Data Submission: To provide necessary safety and usage data to the EPA.
  • 3. Compliance Assessment: To evaluate if the product meets current safety standards.

Frequently Asked Questions

What is the purpose of this form?

This form is meant to evaluate and confirm the eligibility of the pesticide for re-registration.

How do I submit my responses?

Responses can be submitted via email, fax, or traditional mail to the addresses provided in the document.

What happens if I miss the deadline?

Failing to meet the deadline may result in enforcement actions such as product suspension.

Is there a guide on filling out this form?

Yes, detailed instructions are included within the document to assist you.

Can I edit this document?

Absolutely. Use our editor to modify the PDF as needed.

How do I download the edited PDF?

Once you've made your edits, simply click the download button to save the file.

Are there examples of who may need this form?

Yes, pesticide manufacturers, regulatory agencies, and agricultural businesses are among those who may require it.

Can I share this document easily?

Yes, our platform offers simple sharing options for collaborative purposes.

What information do I need to provide?

You need to submit complete and accurate responses regarding your pesticide's usage and compliance.

Is there customer support available?

Yes, you can contact our support team for any questions or issues you may have.

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