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A Risk-based Study Management Approach for Clinical Trial Sites
Sandra “SAM” Sather
On-demand
$279
Analyzing and Understanding ISO 13485 Proposed Changes
Marcelo Trevino
On-demand
$279
Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for Success
Joanna Gallant
On-demand
$279
Avoiding the Top Five Medical Device Clinical Trial Mistakes
Joe Popowicz
On-demand
$279
CE Marking of Medical Devices – A Step-by-Step Guide for Compliance
Rob Packard
On-demand
$279
Competitive Regulatory Strategy for Medical Devices: Win Market Approval While Creating Barriers for your Competition
Michael Drues
On-demand
$279
Conducting the CRO Pre-qualification Audit for GCP Compliance – Key Risk Factors to Avoid
Michael Pierro
On-demand
$279
CRA Oversight – A Risk-based Approach
Sandra “SAM” Sather
On-demand
$279
CRO Selection and Oversight – A Risk-Based Approach
Sandra “SAM” Sather
On-demand
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