CLSI AUTO11 – Information Technology Security of In Vitro Diagnostic Instruments and Software Systems 3rd Edition AUTO11Ed3E
This practical guide compiled with the help of experts from the in vitro diagnostics industry is intended for the laboratory that is creating laboratory developed tests that may be subject to the US Food and Drug Administration (FDA) regulations specifically the Quality System Regulation (QSReg) 21 CFR Part 820.
Product Details
- Edition:
- 3rd
- Published:
- 09/01/2024
- ISBN(s):
- 9781684402533
- Number of Pages:
- 100
- File Size:
- 1 file 6.9 MB
- Note:
- This product is unavailable in Russia Belarus
