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1351. Bioanalytical method validation

1355. Recommendations for clinical laboratory improvement amendments of 1988 (CLIA) waiver applications for manufacturers of in vitro diagnostic devices: guidance for industry and Food and Drug Administration staff

1356. [BIONET annual progress report] (pages 1-25)

1357. [SUMEX renewal application] (pages 126-150)

1358. [SUMEX annual report] (pages 101-125)