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Clinical Trials Adverse Event Reporting Guide - 2020 Edition

$397.00
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Managing Data and Documentation for FDA Inspections - 2019

$397.00
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Design Change Analysis: Five Steps to Compliance

$397.00
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Winning Device EU Marketing Approval: Seven Steps to Writing Clinical Evaluation Reports

Winning Device EU Marketing Approval: Seven Steps to Writing Clinical Evaluation Reports

$397.00
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Using ISO 11607 to Develop Risk-Based Device Packaging

Using ISO 11607 to Develop Risk-Based Device Packaging

$397.00
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Using Social Media in Clinical Trial Recruitment

Using Social Media in Clinical Trial Recruitment

$397.00
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Using the MDSAP Model to Win International Device Approval

Using the MDSAP Model to Win International Device Approval

$397.00
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Understanding the New EU Medical Device Regulations

Understanding the New EU Medical Device Regulations

$397.00
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Unique Device Identifier (UDI) Rule Implementation and Compliance Guide

Unique Device Identifier (UDI) Rule Implementation and Compliance Guide

$397.00
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Use QSIT to Your Advantage in FDA Device Inspections

Use QSIT to Your Advantage in FDA Device Inspections

$397.00
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Understanding Chinas New Medical Device Regulations, 2016 Edition

Understanding China's New Medical Device Regulations, 2016 Edition

$397.00
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Understanding EU Drug Safety Reporting

Understanding EU Drug Safety Reporting

$397.00
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