Conference - Mumbai, India
Key Themes Discussed at this Summit:
• Improving patient care and safety in relation to use of medicines and all medical and paramedical interventions
• Identifying the latest regulatory framework for pharmacovigilance
• Crisis management within drug safety
• Impact of technology – learn and explore
• Explaining how to use the data sources and observational research for effective safety analysis
• Latest developments in pharmacovigilance, drug safety and risk management to ensure safer drugs to market
• Stay ahead of computing and electronic communications in pharmacovigilance
• Risk management plans
• Risk/benefit determinations
• Implications for safety reporting in global clinical trials
• Compliance and drug safety
• Training for drug safety – reporting duties, audits and expectations – risk based inspections
• Safety reporting in licensing agreement
• Good supply chain management practices for medicine distribution
• Accelerating new medicine introduction in developing world & overcoming challenges
• Analyzing the information on current industry projects and trends
• How will PV activities change with clinical trial transformation initiative?
• Recent successful strategies and business models to bring out new medicines
• Exploiting the pharmacy automations and technologies for enhancement of medication safety
• Determining the steps and strategies for enhancing quality in healthcare
• Improving patient care and safety in relation to use of medicines and all medical and paramedical interventions
• Identifying the latest regulatory framework for pharmacovigilance
• Crisis management within drug safety
• Impact of technology – learn and explore
• Explaining how to use the data sources and observational research for effective safety analysis
• Latest developments in pharmacovigilance, drug safety and risk management to ensure safer drugs to market
• Stay ahead of computing and electronic communications in pharmacovigilance
• Risk management plans
• Risk/benefit determinations
• Implications for safety reporting in global clinical trials
• Compliance and drug safety
• Training for drug safety – reporting duties, audits and expectations – risk based inspections
• Safety reporting in licensing agreement
• Good supply chain management practices for medicine distribution
• Accelerating new medicine introduction in developing world & overcoming challenges
• Analyzing the information on current industry projects and trends
• How will PV activities change with clinical trial transformation initiative?
• Recent successful strategies and business models to bring out new medicines
• Exploiting the pharmacy automations and technologies for enhancement of medication safety
• Determining the steps and strategies for enhancing quality in healthcare
• Improving patient care and safety in relation to use of medicines and all medical and paramedical interventions
- Organization: Virtue Insight - Nisha
- For more info on the event and for event brochure kindly visit – http://www.virtueinsight.com/pharma/7th-Pharmacovigilance-2014/
Fri, Nov 21, 2014 - Fri, Nov 21, 2014
Kohinoor Continental Hotel,
Andheri Kurla Road, Andheri East, Mathuradas Vasanji Road, Mumbai, India
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