Bioavailability/Bioequivalence, GCP/GLP, dissolution/BCS, pharmacokinetics, bioanalytics and -statistics

International Conference on Harmonisation Guidelines Development Safety Update Report; E2F: step 4, Aug 2010 (PDF334KB) Structure and Content of Clinical Study Reports; E3: Nov 1995 (PDF471KB) الممارسة السريرية الجيدة; E6(R1): step 4, Jun 1996 (PDF380KB; including IBtemplate) General Considerations for Clinical Trials; E8: Jul 1997 (PDF182KB) Clinical Safety Data Management: Definitions and Standards for Expedited Reporting; E2A: step اقرأ المزيد

العلاج بالخلايا الجذعية في أوكرانيا

Clopidogrel bioequivalence study.Sample.

QUOTATION CLOPIDOGREL 75 Tablets Study design: a two-period, crossover, single-dose bioequivalence study in 36 healthy volunteers of both sexes, clinical confinement during 10 hours before and 32 hours after the dose, 20 blood samples per subject per period will be collected before dosing and till 32 hours after the اقرأ المزيد