Register Now for the Pharmacovigilance World Conference 2023 (London, United Kingdom

DUBLIN, Aug. 8, 2023 /PRNewswire/ — The “Pharmacovigilance World 2023” conference has been added to ResearchAndMarkets.com’s offering.

The Pharmacovigilance World 2023 conference will provide a platform for the participants to discuss, share and stay updated with the present state of affairs in Pharmacovigilance and Drug safety, and how it contributes to 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. Our Pharmacovigilance conferences are known for bringing world-class leaders together to connect, learn and network.

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.

With the augmented incidence of diseases, and the non-medical use of prescription drugs, the incidence of drug abuse has increased enormously in recent years, which is apparent with the excess documentation of adversities and drug toxicities. In this context, drug safety and pharmacovigilance have emerged as a dynamic clinical and scientific discipline to provide adequate information and ensure health safety by the joint interaction of doctors and patients in choosing appropriate treatment methods and drugs.

However, evidence suggests though avoidable, adverse drug reactions (ADRs) to medicines continue to be the bigger life risk. In England, ADR was responsible for up to 6% of hospital admissions, carrying a mortality of 2% and costing the NHS £466 million per annum (€654 million, US$ 602 million) in 2004.

In some countries, ADR is ranked among the top 10 leading causes of mortality. The concept of drug safety and pharmacovigilance has evolved considerably and is highly necessary to keep the severity of ADR under check. In order to prevent or reduce harm to patients and improve public health, it is vital to develop and practice mechanisms for evaluating and monitoring the safety of medicines in clinical use. Pharmacovigilance brief the potential implications of such trends on the evolution of science.

However, these days it is confronting issues to develop a better healthcare system in this global pitch. Some of the major challenges include globalization, web-based sales and information, broader safety concerns, public health versus pharmaceutical industry economic growth, monitoring of established products, developing and emerging countries, attitudes and perceptions to benefit and harm, outcomes and impact, etc.

Who Should Attend:

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.

Conference Streams Include

Global PV & Methodologies
Data Management & Analytics in PV
PV Automation, AI & Machine Learning
Safety Signals & Management
Pharmacovigilance Regulations
Risk Management
Patient-Centric Drug Safety
Case Management
Quality & Compliance
Pharmacovigilance Outsourcing
Medical Devices Safety
Adverse Drug Reactions

KEY DISCUSSIONS WE’LL BE EXPLORING

Pharmacovigilance and globalization
Pharmacovigilance in a pandemic world
Women and child healthcare 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
Risk Evaluation and Mitigation
Adverse drug reaction 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 Workflows with AI & Automation
Other emerging technologies in PV

Attendees include Chief Data Officer, VPs, GMs, Directors, Heads and Managers of

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
Sales and Marketing

For more information about this conference visit https://www.researchandmarkets.com/r/yal32j

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