Description:

This Advance Program in CTM, CDM & PV with PV Database Training is designed to provide an in-depth understanding of the Clinical Trial Management (CTM), Clinical Data Management (CDM), and Pharmacovigilance (PV) domains. The course covers various aspects of CTM, CDM, and PV, including regulations, best practices, data management techniques, adverse event reporting, safety monitoring, PV databases, and reporting tools. Participants will gain practical knowledge and skills to effectively manage clinical trials, handle data for regulatory compliance, and ensure patient safety throughout the drug development process.

Key Highlights:

• Comprehensive training on CTM, CDM, and PV
• In-depth understanding of regulations and best practices
• Practical knowledge on adverse event reporting and safety monitoring
• Hands-on experience with PV databases and reporting tools

What you will learn:

• Master CTM, CDM, and PV
  Gain a thorough understanding of Clinical Trial Management, Clinical Data Management, and Pharmacovigilance domains.
• Compliance and Safety
  Learn about regulations, best practices, adverse event reporting, safety monitoring, and ensuring patient safety.
• PV Databases and Reporting
  Get hands-on experience with Pharmacovigilance databases and reporting tools for effective PV data management.