Handbook of Bioequivalence Testing

Overview

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence ...

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Overview

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence Testing offers a complete description of every aspect of bioequivalence testing.

Features:

  • Describes the current analytical methods used in bioequivalence testing, as well as their respective strengths and limitations
  • Discusses worldwide regulatory requirements for filing for approval of generic drugs
  • Covers GLP, GCP, and 21 CFR compliance requirements for qualifying studies for regulatory submission and facility certification
  • Includes actual examples of reports approved by regulatory authorities to illustrate various scientific, regulatory, and formatting aspects
  • Provides a list of vendors for the software used to analyze bioequivalence studies and recommendations
  • Explains how to apply for a waiver, how to secure regulatory approval of reports, and how to obtain regulatory certification of facilities conducting bioequivalence studies
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Product Details

Table of Contents

Bioequivalence Testing. Regulatory Aspect of Bioequivalence Testing. Pharmacokinetic/Pharmacodynamic Modeling. Waiver of BA/BE Studies. Regulatory Review Process. Statistical Evaluation of Bioequivalence Data. Physicochemical Properties. Drug Delivery Factors. Bioanalytical Method Validation. Good Clinical Practice. Good Laboratory Practice for Nonclinical Lab Studies. Computer and Software Validations. Bioequivalence Reports

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