Get the free Freedom of Information Summary for NADA 141-140 - fda
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This document summarizes the approval of an animal drug application for the combination of Monensin and Bacitracin Methylene Disalicylate used to prevent specific diseases in chickens.
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How to fill out Freedom of Information Summary for NADA 141-140
01
Obtain the Freedom of Information Summary form from the appropriate regulatory agency website.
02
Fill in the applicant's details, including name, address, and contact information.
03
Provide a description of the specific information being requested relevant to NADA 141-140.
04
Include any necessary context or justification for the request.
05
Check for any submission guidelines, such as required signatures or additional documents.
06
Submit the completed form via the specified method (online, mail, etc.) as indicated in the instructions.
Who needs Freedom of Information Summary for NADA 141-140?
01
Individuals or organizations seeking access to information regarding the approval of a new drug application.
02
Researchers looking to analyze the data related to the safety and efficacy of the drug.
03
Pharmaceutical companies interested in regulatory information pertaining to NADA 141-140.
04
Journalists or media professionals investigating pharmaceutical approvals or public health topics.
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The Freedom of Information Act (FOIA), 5 U.S.C. § 552, a disclosure statute, provides that every person has the right to request access to federal agency records or information.
What information cannot be released under FOIA?
Information/data that is NOT covered by the Freedom of Information Act (FOIA) includes: Non-agency records and personal records. Public requests for access to physical artifacts or scientific samples (e.g. core samples, sediment, rocks, fossils, specimen samples, blood samples).
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Failure to respond to a request for records within five working days constitutes a violation of law. Also, withholding records that are not exempt and overcharging for records are violations of the law.
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The Virginia Freedom of Information Act (VFOIA) is the state law governing access by citizens of Virginia, and representatives of the media, to public records and to meetings of public bodies.
What is the freedom of information in Virginia?
The Virginia Freedom of Information Act (VFOIA) is the state law governing access by citizens of Virginia, and representatives of the media, to public records and to meetings of public bodies.
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What is FOIA? Since 1967, the Freedom of Information Act (FOIA) has provided the public the right to request access to records from any federal agency. It is often described as the law that keeps citizens in the know about their government.
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What is Freedom of Information Summary for NADA 141-140?
The Freedom of Information Summary for NADA 141-140 is a document that provides detailed information regarding the approval of a new animal drug, including safety and effectiveness data, production methods, and regulatory status.
Who is required to file Freedom of Information Summary for NADA 141-140?
Manufacturers or sponsors seeking approval for a new animal drug are required to file the Freedom of Information Summary for NADA 141-140.
How to fill out Freedom of Information Summary for NADA 141-140?
To fill out the Freedom of Information Summary for NADA 141-140, applicants must provide comprehensive details about the drug, including dosage form, route of administration, pharmacological data, and any relevant safety studies.
What is the purpose of Freedom of Information Summary for NADA 141-140?
The purpose of the Freedom of Information Summary for NADA 141-140 is to inform the public and veterinary professionals about the safety, efficacy, and quality of a new animal drug, as well as to facilitate transparency in the approval process.
What information must be reported on Freedom of Information Summary for NADA 141-140?
The Freedom of Information Summary for NADA 141-140 must report information such as the drug's active ingredients, intended use, dosage, administration route, manufacturing processes, and results from safety and effectiveness studies.
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