Medical Device Record Retention Fda at Kathryn Lopez blog

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

PPT ICHGCP & FDA Regulations Differences PowerPoint Presentation
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• expected life of device, or • at least 2 years from date of. (b) record retention period. (c) record retention. 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. ensuring that the use of ehr data collected and used as electronic source data in clinical investigations meets fda’s. Persons required to maintain records under this part shall maintain such records for the useful life of. 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.

PPT ICHGCP & FDA Regulations Differences PowerPoint Presentation

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

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