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ELR 2.5.1 Clarification Document for EHR Technology Certification V1.1 Date: October 16, 2012 Co-Authored By: Centers for Disease Control and Prevention And Association of Public Health Laboratories
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The ELR 251 clarification document is a form used to provide additional information or explanations related to a submission made to a regulatory agency.
Any individual or organization that has submitted a document to a regulatory agency and is requested to provide further explanations or details may be required to file an ELR 251 clarification document.
To fill out the ELR 251 clarification document, provide the requested information or explanations in the designated sections of the form following the instructions provided.
The purpose of the ELR 251 clarification document is to ensure that the regulatory agency has all the necessary information and details to make informed decisions or take appropriate actions.
The information to be reported on the ELR 251 clarification document typically includes details or explanations related to the submission in question.
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