8th Global Pharmacovigilance and Drug Safety Summit

Conference Series LLC organizing splendorous Pharmaceutical conferences welcomes you to attend the 8thGlobal Pharmacovigilance & Drug Safety Summit to be held during July 10-11, 2017 in Jakarta, Indonesia focuses on the Advancements in “Pharmacovigilance and risk management”.

The field of Pharmacovigilance is growing by and large, its development is making high impact in field of Pharmaceuticals and medical sciences. 8th Global Pharmacovigilance & Drug Safety Summit focusses on how the importance and significance can be gauged by the fact that it has made huge advancements over the course of time and is continuing to influence..The main theme of 8th Global Pharmacovigilance & Drug Safety Summit is "Innovations in Pharmacovigilance for Systematic Safety and Management"

Sessions Include talks on Drug Safety, Adverse Drug Reactions, Pharmacokinetics and Pharmacodynamics, Pre-Clinical and Clinical Trials, Challenges in Pharmacovigilance, Clinical Trials on Various Disorders, Pharmacovigilance Market, Clinical Research and Statistics, Case Report in Clinical Trials, Pharmacovigilance Significance & Scope, Continental Pharmacovigilance, Good Pharmacovigilance Practice, Pharmacovigilance and Risk Management, Medical devices Pharmacovigilance, Veterinary Pharmacovigilance, Biopharmaceutics, PV Data Base Management, PV Consultings And Bussiness opportunity, Regulatory Affairs, Growth strategies in Pharma, Pharmacy Practices and its Challenges

For more details visit: http://globalpharmacovigilance.pharmaceuticalconferences.com/

Who should attend? Professionals involved in Drug Safety/Pharmacovigilance, Risk Management and REMS, Benefit-Risk Assessment and Communication, Drug Development, Information and Clinical Data Management, Clinical Pharmacology, Clinical Safety, Periodical Safety update Report
Risk Management, Research and Development, Quality Assurance, Patient Safety, Safety Surveillance, Outcomes Research, Data Analysis, Epidemiology, Medical Affairs, Regulatory Affairs and Compliance, Information Technology, Sales and Marketing, Signal management, Pharmacoepidemiology, Risk Management Plans, Benefit-risk assessment, Quality assurance
European Medicines Agency, Clinical practice, Biopharmaceutical and Pharmacokinetics Laboratory Medical Product Safety Assessment, Regulatory Affairs, Clinical Research, Pharmacoepidemiology, Postmarket Studies and Real-World Evidence Generation, Customer Engagement Programs, Medical Information and Medical Communications, Health Outcomes

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