The FDA’s 21 CFR Part 11 guidance on the use of electronic records for data retention or submission is clear. With manually implemented Standard Operating Procedures for Quality Control testing and ...

The FDA’s 21CFR part 11 guidance on the use of electronic records for data retention or submission is clear. With manually implemented Standard Operating Procedures for Quality Control testing and ...

Secondly, the quality control procedures for the operation of SPECT and SPECT/CT systems in routine clinical practice are outlined. The concluding section presents a broad selection of 39 ...