Get the free Agency Information Collection Activities; Submission for Office of Management and Bu...

This document outlines the procedures and requirements for developers of new plant varieties intended for food use to consult with the FDA to ensure compliance with food safety regulations under the

How to fill out agency information collection activities

How to fill out Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties

1. Begin by identifying the relevant forms or documents for the Agency Information Collection Activities.
2. Gather necessary data regarding the foods derived from new plant varieties.
3. Fill out the general information section, including the agency name and contact details.
4. Provide a detailed description of the information collection purpose.
5. Specify the type of information being collected and the methods for collection.
6. Include estimated burden hours for respondents and any associated costs.
7. Identify the statistical methods used for data analysis, if applicable.
8. Submit the completed forms electronically through the appropriate government portal.
9. Monitor for any requests for public comments and be prepared to respond.

Who needs Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

1. Agricultural researchers and scientists involved in developing new plant varieties.
2. Companies and organizations engaged in the production of genetically modified foods.
3. Regulatory agencies needing to review and monitor public health and safety issues.
4. Environmental groups concerned about the implications of new plant varieties.
5. Food manufacturers required to comply with federal regulations on novel foods.

People Also Ask about

How does the FDA regulate the food from genetically engineered plants?

GMO plant developer meets with FDA about a potential new product for use in human and animal food. GMO developer submits food safety assessment data and information to FDA. FDA evaluates the data and information and resolves any issues with the developer.

When did the FDA start regulating food?

1906. The original Food and Drugs Act of 1906 was passed by Congress on June 30th and signed by President Theodore Roosevelt, created to prevent the “manufacture, sale, or transportation of adulterated or misbranded or poisonous or deleterious food, drugs, medications, and liquors”

What is the new protein consultation FDA?

Consultations initiated with the FDA under the early food safety evaluation guidance are designated New Protein Consultations or NPCs. During the consultation, FDA evaluates the developer's Early Food Safety Evaluation of the new non-pesticidal protein produced by the new plant variety under development for food use.

When did the FDA approve GMOs?

1973: Biochemists Herbert Boyer and Stanley Cohen develop genetic engineering by inserting DNA from one bacteria into another. 1982: FDA approves the first consumer GMO product developed through genetic engineering: human insulin to treat diabetes.

Is bioengineered food FDA approved?

FDA regulates most human and animal food, including GMO foods. In doing so, FDA makes sure that foods that are GMOs or have GMO ingredients meet the same strict safety standards as all other foods.

When did the FDA provide additional guidance to the industry on consultation procedures for bioengineered foods?

In 1996, FDA issued Guidance for Industry on Consultation Procedures under FDA's 1992 Statement of Policy for Food Derived from New Plant Varieties.

For pdfFiller’s FAQs

What is Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

It is a process that involves collecting information from stakeholders regarding new plant varieties and ensuring compliance with regulatory frameworks, including obtaining feedback for consultation procedures.

Who is required to file Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

Entities or individuals involved in the development, modification, or commercialization of new plant varieties are typically required to submit information for review.

How to fill out Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

Filing typically involves completing specified forms, providing detailed information about the new plant varieties, and submitting them according to the guidelines outlined by the relevant regulatory agency.

What is the purpose of Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

The purpose is to gather necessary data to assess the safety, environmental impact, and regulatory compliance of new plant varieties before they are approved for commercial use.

What information must be reported on Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Consultation Procedures: Foods Derived From New Plant Varieties?

Information required typically includes details about the plant variety, genetic modifications, potential risks, and methods of development while adhering to the guidelines provided in the consultation procedures.