Complete List of Available Resources

 Book Title

Obtaining Consent in International Clinical Research
2016 Title 21 CFRs 3-Volume Set - Clinical
Clinical Trial Adverse Event Reporting Reference Guide: 2015 Edition
Informed Consent for Clinical Trials
GCP Enforcement Trends
Implementing eConsent for Clinical Trials
Risk-Based Monitoring of Clinical Trials
Mastering New Reporting Rules for Clinicaltrials.gov
Using Social Media in Clinical Trial Recruitment
Global Clinical Trial Trends
Globalization of Sponsored Clinical Trials
Implementing QRM in Clinical Trial Monitoring
Latest Guide for Conducting Pharma Clinical Trials in China
FDA GCP Inspection Preparation: A Primer for Investigative Sites, Sponsors, CROs and IRBs
Guide to the FDA’s Financial Disclosure Requirements for Clinical Investigators
Risk Management to Reduce Protocol Amendments

Webinar Title

Electronic Informed Consent for Biobanks
Data Integrity in Clinical Trials
Reporting Failed Trial Data
Risk-Based Monitoring of Clinical Trials
Gender Disttribution in Device Clinical Trials
Mastering Social Media for Clinical Trials
Clinical Trial Site Quality Management System
GCP Enforcement Trends
Think Like a Clinical Trial Site Auditor
Measuring Suicidality Clinical Trials
Obtaining Consent in International Clinical Trials
Best Practices for Managing Clinical Trial Materials
Data on ClinicalTrials.gov
FDA's New Clinical Biosimilars Guidance
Managing Risk for Clinical Trials
Gender Distribution in Device Clinical Trials

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