Introduction to Good Pharmacovigilance Practices Module 4: Pharmacovigilance Data Management
This introductory course provides a comprehensive overview of Good Pharmacovigilance Practices (GVP), Types of Data Collected in PV, Data Quality and Data Management Principles, Introduction to the General Data Protection Regulation (GDPR) and Signal Detection.
What You Get
Unlimited access to self-paced, online training module that includes learning retention exercises after completion of key topics and a personalized certificate of completion at conclusion of the course.
Who Should Take this Training Course?
This course is recommended for:
- Pharmacovigilance Professionals: Entry-level or junior professionals seeking foundational knowledge of GVP principles.
- Regulatory Affairs Personnel: Individuals involved in regulatory submissions and compliance who need a basic understanding of pharmacovigilance requirements.
- Quality Assurance (QA) and Compliance Officers: Professionals ensuring that pharmacovigilance systems comply with regulations.
- Clinical Research Associates (CRAs) and Coordinators: Individuals involved in clinical trials who need to understand drug safety monitoring and reporting requirements.
- Healthcare Professionals: Physicians, pharmacists, and nurses who play a role in reporting adverse drug reactions.
- Pharmaceutical and Biotech Employees: Professionals from various departments, including R&D, who need a cross-functional understanding of GVP.
- Students and Graduates: Individuals in life sciences, pharmacy, or related fields looking to enter the pharmacovigilance industry.
Materials Provided
Access to the course materials via our online learning platform, certificate of completion.
Prerequisites
None. This course requires you to have internet access. Upon registration, you will be sent access to the course platform to create your account and begin the course.