
The Office of International Activities Records Control Schedules Form
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People also ask
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Who is responsible for ensuring recordkeeping requirements are incorporated in their offices program?
Records managers are responsible for incorporating policies and procedures for the creation of adequate records into the records management program. The records management directive(s) should include guidelines for establishing recordkeeping requirements to ensure the creation of complete and accurate records.
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What is the OSD records disposition schedule?
Records Disposition Schedules documents the major records series (including electronic records) related to the activities of each office, identifies temporary and permanent records, and provides mandatory instructions for the retention and disposition (retirement or destruction) of each records series based on their ...
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What is the FDA record control schedule?
The FDA Records Control Schedules list disposition instructions for records that is unique to FDA. It provides legal disposition instructions for FDA records. These schedules have been approved by FDA and NARA officials.
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What is a records control schedule?
A record control schedule provides for all aspects of records management for a record series including storage, transfer, retention periods, and disposal instructions. All records control schedules will specify a cutoff period.
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What is the meaning of record schedule?
A records schedule is a document that tells you how long to keep specific types of records and tells you what should happen to those records.
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What is a Nara Records schedule?
All records schedules must be approved by NARA. A records schedule provides mandatory instructions for the disposition of the records (including the transfer of permanent records and disposal of temporary records) when they are no longer needed by the agency.
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Who has the authority to approve records schedules?
All records schedules must be approved by NARA. A records schedule provides mandatory instructions for the disposition of the records (including the transfer of permanent records and disposal of temporary records) when they are no longer needed by the agency.
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What is the FDA requirement for record retention?
(b) Records shall be maintained for all components, drug product containers, closures, and labeling for at least 1 year after the expiration date or, in the case of certain OTC drug products lacking expiration dating because they meet the criteria for exemption under § 211.137, 3 years after distribution of the last ...
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