Conference on 9th Pharmacovigilance 2015

Key Topics

• Developing Pharmacovigilance into high quality management system and its components
• Terms of legislation, policies, systems, technology, communication strategies and best practice in PV
• Benchmarking drug safety and pharmacovigilance
• Audit and Inspection: Realistic steps for a fruitful consequence
• How to use the data sources and observational research for effective safety analysis
• Improving patient care and safety in relation to use of medicines and all medical and paramedical interventions
• Safety reporting in licensing agreement
• Drug safety - reporting duties, audits and expectations – risk based inspections
• Challenges and Opportunities in PV lifecycle management
• PV for Biologics – new legislation, new requirements
• Accelerating new medicine introduction in developing world & overcoming challenges
• Good supply chain management practices for medicine distribution
• Determining the steps and strategies for enhancing quality in healthcare
• Developments in Pharmacovigilance, drug safety & risk management to ensure safer drug
• Maintaining proper balance in relationships: Sponsor – Site – CRO & Patients
• Emerging signal detection data gathering successful tools to highlight emerging risks
• Accelerating new medicine introduction in developing world & overcoming challenges
• The developing regulatory framework in advanced and developing markets

Who should Attend

• Pharmaceuticals industry
• Clinical congregation
• Clinical market
• Global clinical market