QPPV Online Training - Technical Training Program To Become A Qualified Pharmacovigilance Professional

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May 07, 2020, 12:45 ET

DUBLIN, May 7, 2020 /PRNewswire/ -- The "QPPV Online Training - A Technical Training Program To Be Qualified Pharmacovigilance Professional (QPPV)" training has been added to ResearchAndMarkets.com's offering.

QPPV stands for Qualified Person Responsible for Pharmacovigilance and is a Qualified and experienced professional in all aspects of Pharmacovigilance. QPPV is the main person responsible for handling the Marketing Authorization Holder's (MAH) Pharmacovigilance system effectively and ensuring the system meet the regulatory obligations in regards to the safety monitoring of the products.

QPPV is required in Pharmacovigilance system as per the legal obligations in EU per GVP Module I which states that all marketing authorization holders to have one qualified person for pharmacovigilance (QPPV) with responsibility for establishing and maintaining all aspects of the company's global pharmacovigilance system. The QPPV is responsible for all Pharmacovigilance related activities like risk management including detection, assessment, understanding and communication of safety information. QPPV acts as a single point of contact for the Competent Authorities for inspections and other communication on a 24-hour basis

At the conclusion of this training, participants should be able to:

Handle the QPPV responsibilities in regards to Pharmacovigilance system management
Create and maintain a Pharmacovigilance system to make it Inspection Ready for regulatory authorities
Overcome challenges in maintenance of the Pharmacovigilance system

If you are already working as QPPV and want to raise your competency standards or looking forward to starting your professional journey as QPPV and looking forward to strengthening your pharmacovigilance management skills, this training will help you to increase your knowledge base regarding the techniques and regulatory processes involved in creation and maintenance of Pharmacovigilance system.

This will be a perfect learning opportunity in all areas of drug safety, pharmacovigilance, regulatory and quality compliance and will be a great addition to your knowledge in pharmacovigilance.

Course Modules:

Regulatory aspects of Pharmacovigilance
Good Pharmacovigilance Practices and Ethical Principles
QPPV and EUDRAVIGIANCE registrations
Regulatory and Legal Requirements in Pharmacovigilance
Pharmacovigilance System management
Pharmacovigilance Operation Management
Pharmacovigilance Risk Management and related activities
Safety Monitoring & Signal Detection
Pharmacovigilance IT system and Validation
Pharmacovigilance Audits and Inspections
Pharmacovigilance Compliance Management
Quality Control (QC) and Quality Assurance (QA)
Pharmacovigilance System Documentations
Pharmacovigilance System Metrics & KPIs Tracking
Pharmacovigilance Training Management
Pharmacovigilance Agreements
Regulatory Reporting
Pharmacovigilance Communication and Reporting
Documentation and Record Keeping
Analytical skills and Decision Making
Communication and Information Management
Workload Management

For more information about this training visit https://www.researchandmarkets.com/r/qfpf4m

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SOURCE Research and Markets