Society of Pharmacovigilance, India

Pharmacovigilance World 2021: November 23-24, 2021 - Two Day Online Conference - ResearchAndMarkets.com

Retrieved on: 
Thursday, June 24, 2021
Health, Pharmaceutical, Pharmaceuticals policy, Health, Drug Safety, Clinical research, Clinical trials, Health care quality, Pharmacovigilance, Drug Safety, Society of Pharmacovigilance, India

The "Pharmacovigilance World 2021" conference has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Pharmacovigilance World 2021" conference has been added to ResearchAndMarkets.com's offering.
  • The Pharmacovigilance World 2021 conference will provide a platform for the participants to discuss, share and stay updated with present state of affairs in Pharmacovigilance and Drug safety, and contribute to the public health.
  • It will also allow all its participants to interact with the experts, discuss the various developments, challenges faced and innovations in the field.
  • The concept of drug safety and pharmacovigilance has evolved considerably and is highly necessary to keep the severity of ADR under check.

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

Retrieved on: 
Thursday, May 7, 2020
Pharmaceuticals policy, Health, Articles, Healthcare quality, Drug Safety, Qualified Person Responsible For Pharmacovigilance, Clinical research, Pharmacovigilance, Marketing authorization, GVP, Society of Pharmacovigilance, India

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.

Key Points: 
  • 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 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.