Introduction to Good Pharmacovigilance Practices Level 1 – Module 2: Regulatory Framework for Pharmacovigilance
Understanding Good Pharmacovigilance Practices
This continuation course provides additional insight into the regulatory framework of Good Pharmacovigilance Practices (GVP), the guidelines and principles that ensure the safety and efficacy of medicinal products throughout their lifecycle. Participants will explore the fundamental concepts, regulatory requirements, and best practices in pharmacovigilance, gaining insights into the processes that protect patient health by monitoring and managing drug safety risks. By the end of this course, learners will have a solid understanding of GVP principles and the critical role they play in the pharmaceutical industry.
Our Training Approach
Our team of expert consultants and trainers has designed online training courses to help you understand the key principles of GVP so that you can ensure your organization is meeting regulatory requirements. By utilizing an online, self-paced platform, you can complete the training when it is convenient for you.
After purchasing this course, you will get access to course materials in the online portal within 1 business day.
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 the conclusion of the course.
Who Should Attend Good Pharmacovigilance Training?
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:
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.
Course Number: GVPTWO100
Duration: Self-paced online course, approximately 45 minutes
Cost: $50 per student
Group Pricing: For groups of 10 or more, please contact us for pricing.
Purchase This Online Course Below to Gain Access to the Materials:
Interested in other on-demand courses? Check out our GxP Compliance and other technical e-learning courses, here.
