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EDGAR: Extraction of Drugs, Genes And Relations from the Biomedical Literature Thomas C. Rindflesch Lister Hill Center, National Library of Medicine Bldg. 38A, MS-54, Bethesda, MD 20894 TCR LHC.elm.NIH.gov
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Edgar extraction of drugs is a process of collecting and extracting information related to drug filings from the Electronic Data Gathering, Analysis, and Retrieval (EDGAR) system maintained by the U.S. Securities and Exchange Commission (SEC).
Pharmaceutical companies and drug manufacturers are required to file edgar extraction of drugs. They need to submit the necessary information related to their drug filings to the SEC via the EDGAR system.
To fill out edgar extraction of drugs, pharmaceutical companies and drug manufacturers need to access the EDGAR system provided by the SEC. They should input the required information, including details about their drug filings, such as drug names, FDA approval status, clinical trial results, and any other relevant information.
The purpose of edgar extraction of drugs is to ensure transparency and accessibility to information regarding drug filings. It allows investors, researchers, and the general public to access and analyze data related to pharmaceutical products and their regulatory compliance.
On edgar extraction of drugs, pharmaceutical companies and drug manufacturers are required to report information such as the names of their drugs, FDA approval status, clinical trial results, adverse events, safety warnings, and any other relevant information related to their drug filings.
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