3rd adverse events reporting safety strategies and capa summit

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The 3rd Adverse Events Reporting, Safety Strategies and CAPA Summit will offer an in-depth analysis of benefit-risk assessments, real-world data, risk management plans, signal detection, periodic reporting and solicited/unsolicited reports, all while working toward the goal of improving the safety strategies implemented by your company.

Top Five Reasons to Attend

  1. Hear from industry leaders about the latest developments in the pharmacovigilance and drug safety world and how best to optimize your safety processes
  2. Discuss ways to achieve efficient reporting of adverse events from traditional and non-traditional sources and optimize signal detection and management
  3. Explore where structured benefit-risk assessments can be used to improve decision-making and why this matters for pharma, regulators and patients
  4. Learn about measuring risk management activities for the identification and prevention of adverse events, from clinical to postmarket phases, and conducting the right CAPAs (Corrective and Preventive actions)
  5. Hear about the impact of the European pharmacovigilance legislation and how companies are implementing it
  6. This conference is designed for professionals from pharmaceutical, biotech and medical device companies with responsibilities in the following areas:

Pharmacovigilance

  • Drug Safety.
  • Risk Management.
  • Safety Research/Epidemiology.
  • Good Clinical Practice (GCP) Compliance.
  • Pharmacoepidemiology.
  • Medical Product Safety Assessment.
  • Regulatory Affairs.
  • Clinical Research.
  • Clinical Development.
  • Clinical Auditing.
  • Safety Surveillance.
  • Signal Detection.
  • Clinical Safety.
  • Quality Assurance and Control.
  • Quality Systems and Processes.
  • Patient and Medical Safety.
  • Case Management/Review.
  • Health Outcomes.
  • Data Management/Analysis.
  • Phase IV/Postmarketing Studies.
  • Research and Development.
  • Trial Optimization. [1]

This event is also of interest to:

  • CRM/Data Management Software Vendors.
  • Audit Tracking and Management Vendors.
  • Technology Vendors/Portal Service Providers.
  • Adverse Event/Case Management Service Providers.
  • Safety Database Providers for Case Management.
  • Clinical Research Organizations (CROs).
  • Service Providers for Drug Safety.
  • Regulatory/Healthcare/Pharmacovigilance Consultants.
  • Compliance/Quality Assurance/GCP Consultants.
  • Healthcare Translation Agencies. [1]

Top Photos

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Speaker Highlights

Agenda

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Fun things happened

Source

  1. 1.0 1.1 http://info.exlevents.com/rs/195-NER-971/images/C822_web.pdf?aliId=356458858

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