Medical Device Record Retention Fda at Clara Stamps blog

Medical Device Record Retention Fda. All records required by this part shall be retained for a period of time equivalent to the design. Persons required to maintain records under this part shall maintain such records for the useful life of. (b) record retention period. the useful life of a device is the time a device is in use or in distribution for use. • expected life of device, or • at least 2 years from date of. Retain all records required by part 820 for: For example, a record may be retired if the person. all records required by this part shall be retained for a period of time equivalent to the design and expected life of the device, but in. (c) record retention. An investigator shall retain records required to be maintained under this part for a period of 2. § 821.60 retention of records. ensuring that the use of ehr data collected and used as electronic source data in clinical investigations meets fda’s.

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For example, a record may be retired if the person. • expected life of device, or • at least 2 years from date of. § 821.60 retention of records. ensuring that the use of ehr data collected and used as electronic source data in clinical investigations meets fda’s. All records required by this part shall be retained for a period of time equivalent to the design. An investigator shall retain records required to be maintained under this part for a period of 2. all records required by this part shall be retained for a period of time equivalent to the design and expected life of the device, but in. the useful life of a device is the time a device is in use or in distribution for use. Retain all records required by part 820 for: (b) record retention period.

PPT Retention of Medical Records Law PowerPoint Presentation, free

Medical Device Record Retention Fda the useful life of a device is the time a device is in use or in distribution for use. All records required by this part shall be retained for a period of time equivalent to the design. § 821.60 retention of records. all records required by this part shall be retained for a period of time equivalent to the design and expected life of the device, but in. • expected life of device, or • at least 2 years from date of. (c) record retention. Retain all records required by part 820 for: ensuring that the use of ehr data collected and used as electronic source data in clinical investigations meets fda’s. (b) record retention period. For example, a record may be retired if the person. An investigator shall retain records required to be maintained under this part for a period of 2. the useful life of a device is the time a device is in use or in distribution for use. Persons required to maintain records under this part shall maintain such records for the useful life of.

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