ASCEND BY NTHRYS
Research Abroad Products

Pharmacovigilance Workshops

Click a category to proceed further.

Showing 1–12 of 50 categories
Adverse Event Reporting Fundamentals
Essential training for professionals learning to identify, document, and report adverse events through standardized pharmacovigilance systems and databases.
Explore workshops →
MedDRA Coding and Classification
Specialized course teaching MedDRA terminology application for accurate classification and coding of adverse event reports for regulatory compliance.
Explore workshops →
ICH Guidelines for Drug Safety
Comprehensive program covering International Council for Harmonisation guidelines and standards essential for global pharmacovigilance operations.
Explore workshops →
Spontaneous Adverse Event Monitoring
Practical training for professionals managing unsolicited adverse event reports from healthcare providers and patients through various reporting channels.
Explore workshops →
Pharmacovigilance Software Systems Training
Hands-on workshop teaching operation of industry-standard pharmacovigilance software platforms and electronic case tracking systems.
Explore workshops →
Signal Detection and Analysis Methods
Advanced training for specialists learning statistical methods and software tools to identify potential drug safety signals from adverse event data.
Explore workshops →
Risk Management Planning and Assessment
Strategic program teaching development and implementation of Risk Minimization Action Plans for pharmaceutical products and safety risk mitigation.
Explore workshops →
Serious Adverse Event Case Processing
Specialized training for professionals handling urgent serious adverse event reports requiring rapid assessment, investigation, and regulatory notification.
Explore workshops →
Post-Marketing Surveillance Operations
Comprehensive course covering post-approval safety monitoring systems, data collection protocols, and ongoing surveillance program management.
Explore workshops →
Regulatory Compliance and Documentation
Essential training for professionals ensuring pharmacovigilance activities meet regulatory requirements and maintain complete audit-ready documentation.
Explore workshops →
Clinical Trial Safety Reporting
Specialized program teaching safety event reporting requirements, timelines, and protocols specific to clinical trial pharmacovigilance.
Explore workshops →
Data Quality Assurance and Validation
Practical workshop for technicians learning verification, validation, and quality control procedures for adverse event data integrity.
Explore workshops →