Description

The Pharmacovigilance & Drug Safety event is designed to bring you a unique opportunity to gain fresh insights into the common issues faced in the industry, highlighting the areas with the need to focus on in order to remain compliant. Moreover this conference stream will provide the opportunity to network with various industry professionals including pharmaceuticals, biologics, devices, CROs and PV service providers.

Pharmacovigilance & Drug Safety event 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.

Key Practical Points

  • Impacts of PV on Covid-19
  • Improving Signal surveillance
  • Artificial Intelligence in Signal Detection
  • Combination products – Regulation, trials, and risk management
  • The role of data mining in Pharmacovigilance and its benefits
  • IDMP standards and strategy
  • Developing a pharmacovigilance risk management plan with a risk minimization action plan (RiskMAP) for high risk products
  • Understanding how Artificial Intelligence is transforming pharmacovigilance
  • Evaluation of quality and manufacturing in production
  • Audits and Inspections
  • Strengthening Pharmacovigilance quality management system
  • Impact of AI in Pharmacovigilance
  • Upcoming regulatory changes
  • Signal management
  • Application of data analytics in Pharmacovigilance processes to increase speed of signal detection
  • Cooperation for patients safety
  • Development and deployment of advanced data management systems
  • Does AI have a real role to play in PV?
  • The role of surveys in controlling the overall risk management system
  • Proactive vs. predictive technologies in the future of PV
  • Brexit and the impact on pharmacovigilance
  • Strategies to improve PV
  • Real World Evidence in PV
  • Best practices for developing an overall PV audit strategy with a business partner
  • Is there a way to effectively and reliably use social media towards a QPPV’s end goals?
  • Real-time drug safety data analysis in medical monitoring
  • How has inspection preparation changed and what are the new methods on the horizon?
  • Big data and AI in pharmacovigilance
  • Pharmacovigilance Monitoring and automation in Social media

Who should attend?

Members of board, C-level, Senior Vice Presidents, Vice Presidents, Directors and Heads of departments from pharmaceutical/biotechnology industry / industries involved in:

  • QPPV
  • Risk Management
  • Pharmacoepidemiology
  • Signal Detection
  • Pharmacovigilance
  • Risk Assessment
  • Market Research Programs
  • PV Governance
  • Phase IV/Postmarketing Safety
  • Drug Safety
  • Patient Safety
  • Medical Affairs
  • Quality Assurance
  • Regulatory Affairs
  • Audit Readiness
  • Medical Safety
  • Safety Surveillance

Exhibitors & Sponsors

Booth #H3

IMP Logistics

IMP Logistics is a specialized logistics and warehousing provider, and has been present in the industry of clinical trial logistics services and supply chain management for more than 15 years servicing a region of 500+ million people. We are equipped with the best knowledge and expertise to support clinical trial projects with comprehensive warehousing and distribution services in the most challenging countries.

Our coverage area currently reaches out to Russia, Ukraine, Belarus (where we have our own offices and depots) as well as Georgia, Moldova, Serbia, Israel, Turkey, Taiwan, Philippines, South Africa and South Korea (operated by our depot partners).

IMP Logistics customers are top pharmaceutical and global healthcare logistics companies, local and global CROs we’ve been cooperating for years.

Our experience is more than 5 000 projects we supported worldwide with the following services for clinical trials:

  • Regulatory support;
  • Import and export;
  • Storage and warehousing;
  • Nationwide and international distribution;
  • Clinical trial material destruction;
  • Comparator sourcing;
  • Additional labeling services;
  • Clinical trial packaging;
  • Clinical trial logistics project management.

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