Toronto, Canada (PRWEB) January 15, 2013
Effectiveness and safety observed in real-life can differ significantly from efficacy and safety observed in clinical trials. Not only can this create treatment and safety gaps, but it can undermine return on investment for drug developers and efficient use of funds for both public and private healthcare providers and payers.
Post-Approvals Clinical & Epidemiology Studies (PACES), including those using healthcare administrative databases analysis, are sources of information that allow the assessment of real-life effectiveness. Pharmaceutical companies, insurers, payers and benefits managers are increasingly using these databases to conduct observational studies to generate evidence. Using real-life administrative databases could help close the treatment and safety gaps created by the intrinsic differences between clinical trials and real-life utilization of drugs.
Attendees will get the answers to questions, including:
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Karen Lim (416) 977-6555 ext 227