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GCP Questions, FDA Answers, 2022 Edition

GCP Questions, FDA Answers, 2022 Edition

$397.00
Focus on running compliant trials, not on searching for how best to do it. Let GCP Questions, FDA Answers guide you. Read More

Books

Perspectives on Clinical Trial Agreements

Perspectives on Clinical Trial Agreements: What Sites, Sponsors and Stakeholders Need

$397.00
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Data Privacy and Research Transparency

Data Privacy and Research Transparency: Balancing Opposing Priorities

$397.00
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Best Practices for Clinical Trial Site Management

Best Practices for Clinical Trial Site Management

$79.00
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GCP Questions, FDA Answers, 2021 Edition

GCP Questions, FDA Answers, 2021 Edition

$397.00
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Surviving an FDA GCP Inspection

Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

$397.00
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Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

$397.00
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Data Integrity in Clinical Trials

Data Integrity in Clinical Trials: Ensuring Valid Results

$397.00
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Billing Sponsors for Site Expenses: How to Budget, Handle and Track Payments

Billing Sponsors for Site Expenses: How to Budget, Handle and Track Payments

$397.00
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Guide to Informed Consent Compliance

Guide to Informed Consent Compliance

$397.00
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Data Privacy in the EU

Data Privacy in the EU: A Guide for Clinical Trial Sponsors and Sites

$397.00
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Risk-Based Monitoring of Clinical Trials 2017 – New Trends and Best Practices : PDF

Risk-Based Monitoring of Clinical Trials 2017: New Trends and Best Practices

$297.00
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The Revised ICH E8: A Guide to New Clinical Trial Requirements

The Revised ICH E8: A Guide to New Clinical Trial Requirements

$397.00
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