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Now Taking Orders for Our April 1, 2005 Books!        ALSO Check Out our Books with the ICH E6(R3) GUIDELINE FOR GOOD CLINICAL PRACTICE       See our BOOKSTORE Drop-Down Menu for included titles

GCP for Drug Studies Books

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Book CG1-E6R3: 2025 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials (With ICH GCP E6(R3)) Book CG1-E6R3: 2025 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials (With ICH GCP E6(R3)) - $ 46.95
Book CG1: 2025 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials Book CG1: 2025 Comprehensive Clinical Research Desk Reference for Drug and Medical Device Trials - $ 45.95
Book 1A-E6R3: 2025 Selected Regulations & Guidance for Drug Studies (With ICH E6(R3)) Book 1A-E6R3: 2025 Selected Regulations & Guidance for Drug Studies (With ICH E6(R3)) - $ 24.95
Book 1A: 2025 Selected Regulations & Guidance for Drug Studies Book 1A: 2025 Selected Regulations & Guidance for Drug Studies - $ 22.95
Book 1B-E6R3: 2025 FDA Good Clinical Practice Guide (With ICH GCP E6(R3)) Book 1B-E6R3: 2025 FDA Good Clinical Practice Guide (With ICH GCP E6(R3)) - $ 26.95
Book 1B: 2025 FDA Good Clinical Practice Guide Book 1B: 2025 FDA Good Clinical Practice Guide - $ 24.95
Book 1C-E6R3: 2025 Good Clinical Practice Regulations in the US & the EU (With ICH GCP E6(R3)) Book 1C-E6R3: 2025 Good Clinical Practice Regulations in the US & the EU (With ICH GCP E6(R3)) - $ 24.95
Book 1C: 2025 Good Clinical Practice Regulations in the US & the EU Book 1C: 2025 Good Clinical Practice Regulations in the US & the EU - $ 22.95
Book 3A: 2025 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor Responsibilities Book 3A: 2025 Selected Regulations and Guidance on Protection of Human Subjects: Clinical Investigator, IRB & Sponsor Responsibilities - $ 22.95
Book M1: 2025 Mini Pocket-Sized (3" x 5") ICH Guidelines for GCP (E6) and Clinical Safety Data Management (E2A) Book M1: 2025 Mini Pocket-Sized (3" x 5") ICH Guidelines for GCP (E6) and Clinical Safety Data Management (E2A) - $ 12.95
Book M2: 2025 Mini Pocket-Sized (3" x 5") Code of Federal Regulations on Good Clinical Practice, 21 CFR Parts 11, 50, 54, 56, 312 (Does not include Part 314 or any ICH Guidelines) Book M2: 2025 Mini Pocket-Sized (3" x 5") Code of Federal Regulations on Good Clinical Practice, 21 CFR Parts 11, 50, 54, 56, 312 (Does not include Part 314 or any ICH Guidelines) - $ 12.95
Book 3D: 2025 Common Terminology Criteria for Adverse Events (CTCAE) Book 3D: 2025 Common Terminology Criteria for Adverse Events (CTCAE) - $ 13.95
Book 13: 2025 FDA Guidance on Clinical Study Reports and Statistical Principles for Clinical Trials (Copy) Book 13: 2025 FDA Guidance on Clinical Study Reports and Statistical Principles for Clinical Trials (Copy) - $ 17.95
Book 25: 2025 Laws, Regulations, and Guidance on Pediatric Studies Book 25: 2025 Laws, Regulations, and Guidance on Pediatric Studies - $ 17.95
Book M4: 2025 Mini Pocket-Sized (3" x 5") Clinical Research Dictionary Book M4: 2025 Mini Pocket-Sized (3" x 5") Clinical Research Dictionary $ 12.95
Book 3B: 2025 Selected Documents on International Ethical Conduct, Federalwide Assurances, & OHRP Compliance in Academic Research Book 3B: 2025 Selected Documents on International Ethical Conduct, Federalwide Assurances, & OHRP Compliance in Academic Research $ 17.95
Book 14: 2025 Selected Recently-Finalized FDA Guidance Documents Book 14: 2025 Selected Recently-Finalized FDA Guidance Documents $ 18.95
Book 16: 2025 Preambles to Good Clinical Practice Regulations Book 16: 2025 Preambles to Good Clinical Practice Regulations $ 28.95
Book 3C: 2024 The Official Investigator's Handbook for Conducting Cancer Clinical Trials Book 3C: 2024 The Official Investigator's Handbook for Conducting Cancer Clinical Trials $ 18.95