European Pharmacovigilance & Clinical Trials 2016

European Pharmacovigilance & Clinical Trials 2016 is a conference dedicated to the key issues, various developments, challenges and innovations in the field of Pharacovigilance and Clinical Trials.

Key Topics

• PV regulations and challenges
• Harmonization and Pharmacovigilance
• Risk management and minimization
• The new EU legislation on clinical trials, its impact and future
• Signal detection and post authorization safety
• Adverse drug reactions reporting
• Clinical data management
• Business development and models in clinical trials
• IT and new technologies for improvement of PV and clinical research
• Good Clinical Practices and Good Pharmacovigilance practices
• Strategies to improve clinical trials and PV

Who should Attend

Attendees involved or interested in:

• Directors
• VPs
• CEO`s
• Heads
• CIO`s
• CTO`s
• Vice Presidents
• Presidents
• Heads & Managers
• Directors
• Consultants and professionals in the following Healthcare policy makers Healthcare practitioners Pharmaceutical industry scientists
• Scientific Advisors
• Executives Executives and scientists from clinical research organizations Contract outsourcing service providers IT consultants
• Researchers