Clinical Trials & Good Clinical Practices (GCP) Training
Showing 81–96 of 110 results
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Writing Clinical Monitoring Reports: Using the Liquid Report Writing Method
$279.00 – $2,550.00 Select options -
Source Data Review (SDR) vs. Source Data Verification (SDV) – A Site Monitoring Best Practices Update
$279.00 – $2,550.00 Select options -
Root Cause Analysis for Clinical Research Professionals
$279.00 – $2,550.00 Select options -
Risk-Based Monitoring Plan Development
$279.00 – $2,550.00 Select options -
Remote Monitoring of Clinical Source Data – Why Not?
$279.00 – $2,550.00 Select options -
Remote Monitoring Implementation Post ICH GCP E6 (R2): A Practical Guide
$279.00 – $2,550.00 Select options -
The Power of Influencing – Achieving Patient-focused Outcomes to Guarantee Success
$279.00 – $2,550.00 Select options -
Building Accountability on Your Clinical Teams
$279.00 – $2,550.00 Select options -
Identifying and Closing the Training Gap in Clinical Research
$279.00 – $2,550.00 Select options -
Course Vouchers – 10 Pack
$1,649.00 Add to cart -
Sale!
Course Voucher – 5 Pack
$949.00 Add to cart -
Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for Success
$279.00 – $2,550.00 Select options -
Monitoring Medical Device / ISO 14155 GCP
$279.00 – $2,550.00 Select options -
Document Authoring, Archive, and Inspection – Challenges And Tips For Establishing Audit-Proof Processes
$279.00 – $2,550.00 Select options -
Change Management Plan Development for Risk-Based Clinical Studies: From Site Monitoring to Vendor Management and Beyond
$279.00 – $2,550.00 Select options -
Understanding The New NIH/HHS Final Rule On Clinical Trial Reporting – Tips For Compliance Success
$279.00 – $2,550.00 Select options