Controlling type 1 error rate for sequential, bioequivalence studies with crossover designs. [electronic resource]
Producer: 20190314Description: 96-105 p. digitalISSN:- 1539-1612
- Computer Simulation
- Cross-Over Studies
- Data Accuracy
- Data Interpretation, Statistical
- Drug Compounding
- Humans
- Models, Statistical
- Pharmaceutical Preparations -- administration & dosage
- Randomized Controlled Trials as Topic -- methods
- Research Design -- statistics & numerical data
- Sample Size
- Therapeutic Equivalency
- Treatment Outcome
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Publication Type: Journal Article
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