Effect of length of sampling schedule and washout interval on magnitude of drug carryover from period 1 to period 2 in two-period, two-treatment bioequivalence studies and its attendant effects on determination of bioequivalence

Author:

Dhariwal Kuldeep,Jackson Andre

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine

Reference9 articles.

1. Design and Analysis of Bioavailability and Bioequivalence Studies. Marcel Dekker: New York 1992; 30: 50.

2. Guidance for Industry: Bioavailability and Bioequivalence Studies for Orally Administered Drug Products-General Considerations. Food and Drug Administration, October 27, 2000.

3. 1982. Pharmacokinetics, 2nd edn Marcel Dekker: New York, 1982; 5: 297.

4. Planning of Experiments. Wiley: New York, 1958.

5. Experimental Designs. Wiley: New York, 1957.

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