Good Pharmacovigilance Practices (GVP): Updates to the European Union GVP Guidelines
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Download 2024 UPDATE:
This program is currently unavailable for enrollment.
It may have been updated or discontinued.
Check for newer version in our catalog.
This program is currently unavailable for enrollment.
It may have been updated or discontinued.
Check for newer version in our catalog.
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Free Trial CoursesOutline:Course Introduction -Course Overview -What Students will Learn EU GVP Update Process -EU GVP Update Process Changes in Pharmacovigilance - Brexit Transition -General Principles of Post-Brexit UK Pharmacovigilance -Knowledge Check EU GVP - Recent Updates -Module l -Module ll -Module lll -Module lV -Module V -Module Vl -Module Vl - Addendum l -Module Vll -Module Vlll -Module Vlll - Addendum l -Module Xl -Module Xl - Addendum 1 -Module X -Module XV -Module XVl -Module XVl - Addendum l Updates to GVP Modules Covering Major Pharmacovigilance Processes -Quick Knowledge Check -Updates to Chapters On Product-Or Population-Specific Considerations -Product-or Population-Specific Considerations I - Vaccines for Prophylaxis Against Infectious Diseases -Product-or Population-Specific Considerations II - Biological Medicinal Products -Product-or Population-Specific Considerations IV - Pediatric Population Updates to GVP Chapters On Product-Or Population-Specific Considerations Quick Knowledge Check -Final GVP Annexure Updates -GVP Annex I -GVP Annex II - Templates -Final GVP Annexure Additions -GVP Annex III - Other Pharmacovigilance Guidance -Note For Guidance - Eudravigilance Human - Processing Of Safety Messages And Individual Case Safety Reports (ICSRS) -GVP Annex IV -GVP Annex V Final GVP Annexure Updates and Additions Quick Knowledge Check Conclusion -What We Covered Test Your Knowledge -Results Certification of Completion | Objectives:This course will provide students with a robust introduction to all modules of GVP, enabling you to understand the impact of the GVP modules throughout the pharmacovigilance landscape. | |
This Course is Included in the Following Professional Certification Program(s):
 | Good Pharmacovigilance Practices (GVP) Professional Certification ProgramProgram ID: GVProPrice: $695.00 (USD) |
Benefits of Being Certified from Biopharma Institute: Throughout our training students will be engaging in active learning using interactive eLearning modules validated by 3rd party organizations for relevancy, compliance, and regulatory content. Courses are developed by subject matter experts (SMEs) and instructional design professionals with the goal to promote the students' retaining of key knowledge. The programs further offer access to regulatory references, real-life case studies, and introduce other important information necessary to assist with learning. Since 2003, Biopharma Institute has been aiding both professionals and their corporate employers with fulfilling training requirements. Biopharma Institute's certifications are recognized by a wide spectrum of industries, regulators, and companies around the world. Furthermore, our training solutions are customizable to any organization's training needs. Today, Biopharma Institute offers over 300 courses training on clinical research, drug manufacturing (cGMP), regulatory affairs, validation systems, pharmacovigilance, good laboratory practice (GLP), and data integrity. We supply our training to clinical research, pharmaceutical, and medical device industries.
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