Pharmacovigilance World 2020 is about to happen

03-04 June 2020 London United Kingdom


The Pharmacovigilance World 2020 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 conference will bring-forth the participants and the representatives from various fields of pharmacovigilance and drug safety under a common umbrella, and will provide them an opportunity to network with various industry professionals including pharmaceuticals, biologics, devices, CROs and PV service providers.

KEY HIGHLIGHTS
· Pharmacovigilance and globalization
· Women and child health care medicines and pharmacovigilance
· Patient-centric approaches in PV
· Pharmacovigilance legislation and regulations
· Harmonization and pharmacovigilance
· Advanced therapeutic techniques and pharmacovigilance
· Pharmacovigilance and data management and eudravigilance
· Post-marketing surveillance in pharmacovigilance
· PV regulations and challenges
· Benefit-risk management strategies
· Risk management and minimization
· Adverse drug reactions reporting
· Signal detection and post authorization safety
· Good Pharmacovigilance Practices
· Innovative approaches to drug safety
· Strategies to improve PV
· Real World Evidence in PV
· Big data and AI in pharmacovigilance
· Pharmacovigilance Monitoring and automation in Social media
· Other emerging technologies in PV
WHO SHOULD ATTEND THE CONFERENCE
CEOs, CTOs, CIOs, Presidents, Vice Presidents, Directors, Heads & Managers, Scientific Advisors, Consultants and professionals who work for pharmaceutical, biotechnology & devices industries, CROs and service providers involved in Pharmacovigilance and Drug safety.
· Pharmacovigilance
· Safety & Risk management
· Drug safety
· PV Compliance
· Safety Surveillance
· Medical Affairs
· Regulatory Affairs
· Inspection and Audit
· Pharmacoepidemiology
· Post-market studies
· Medical product safety assessment
· Drug Research & Development
· Clinical Pharmacology
· Medical information
· Contract outsourcing service providers
· Health outcomes
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