All Courses
Showing 33–48 of 249 results
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Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
$279.00 – $2,550.00 Select options -
FDA Compliant QC and QA Practices: Creating a Perfect, Audit-Ready QMS
$279.00 – $2,550.00 Select options -
The EU General Data Protection Regulation (GDPR): What US Pharma/Biotech Companies Need to Know to Comply
$279.00 – $2,550.00 Select options -
The Core Competencies of a World-Class Medical Affairs Team
$199.00 – $1,695.00 Select options -
Executing Proper Event Investigations: Critical Steps In Ensuring Compliant Corrective Actions
$279.00 – $2,550.00 Select options -
FDA Guidance for Industry “Process Validation: General Principles & Practices” – Whatever Happened to IQ, OQ, PQ?
$279.00 – $2,550.00 Select options -
Measuring CAPA Effectiveness: Critical Tips in Getting the Right CAPA and Showing It Works
$279.00 – $2,550.00 Select options -
Biocontainment For Manufacturing: Understanding The Risks, Guidance, and Design Requirements
$279.00 – $2,550.00 Select options -
Note to File 101: Critical Steps for When, and When Not To, Engage in NTFs
$279.00 – $2,550.00 Read more -
Right to Try Legislation: Impact on Industry, Health Authorities, and Patients
$279.00 – $2,550.00 Select options -
Building a Best in Class Medical Affairs Organization: Strategies for Success
$199.00 – $1,695.00 Select options -
The Value of the Medical Affairs Organization: A Comprehensive Overview
$199.00 – $1,695.00 Select options -
FDA Regulations for Analytical Instrument Qualification and Validation: Comprehensive Best Practices
$279.00 – $2,550.00 Select options -
Mock Regulatory Inspections: How to Get the Best Bang for Your Buck
$279.00 – $2,550.00 Select options -
Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11
$279.00 – $2,550.00 Select options -
Key Elements of Pharmaceutical Serialization and Track & Trace Systems
$279.00 – $2,550.00 Select options