Book CG1: 2026 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials <span style="color: #b70202">(With FDA/ICH GCP E6(R3))</span>Description Contents Cover Our best selling Book updated with ICH E6(R3)*, this book contains the key documents that cover clinical research in drug and medical device trials for sponsors, investigators coordinators, and IRBs. At over 750 pages, this spiral bound, 5. 5" x 8" book contains regulations and guidance documents from the FDA and OHRP, covering topics that could previously only be obtained by buying 5 different books. Please see the

5" book is a re-formatted printing of the book

The Rules Governing Medicinal Products in the EU

Laboratory Controls

Manufacturing and Quality Assurance

Children Involved as Subjects in Research (As of April 1

• Investigational New Drug Applications and New Drug Applications

• 750+ copies:  $30

• No further changes are planned

95          • 500+ copies:  $18

• FDA Guidance for Industry:  Electronic Systems

E6(R3) FDA/ICH Good Clinical Practice Guidance (US Step 5)

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