Webinar On Patient Compliance in Drug Trials

1. ContactUs:416-915-4458 WeEmpower,YouComply! Webinar On Patient Compliance in Drug Trials ProductId ProductId Product Id : FDB1321 Category : Food, Drugs & Biologics Category Category Food, Drugs & Biologics Food, Drugs & Biologics ScheduledOn Scheduled On Scheduled On : Thursday, July 17, 2014 at 13:00 Hrs Thursday, July 17, 2014 at 13:00 Hrs ScheduledOn Scheduled On Monday, June 16, 2014 at 13:00 Hrs Duration Duration Speaker Dr. NaginaParmar Duration Duration 60 Minutes 60 Minutes Toregisterforthiswebinarvisitourhttps://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1321 Webinar Description: This 1 hour virtual seminar will help you understand compliant issues researchers face while conducting clinical trials especially in the drug trials. Research subjects who are enrolled in the clinical trials need to have the better idea of how important the compliance for the success coordination of trials and also for the betterment of clinical care. Research subjects who are not compliant with their treatment will have to complete extra visits associated with the adverse events they will have if they don’t take their medicine regularly. The issues and challenges associated with these compliant issues will be discussed. Also the tools and resources that are available for researchers to overcome these challenges will be identified. Thousands of articles have been published with vast amount of research been done on this issue. Compliance, in other words adherence in patients, is a big problem in the patient populations who participate in research. For them, taking medicine during their participation in the research is not important since this was never reinforced by their providers. The studies have been done over the past 25 years especially identifying the causes of noncompliance, exploring possible solutions, identifying adherence with respect to specific diseases, identifying the patients, investigator’s, pharmacist and Physician’s roles with respect to compliance. Areas Covered in the Session: • Upon completion of this webinar, attendees should be able to: • Understand about the definition of compliance • Understand the history behind it • Identify the issues associated with the compliance in the drug trials • Identify the challenges associated with the compliance in the drug trials • Determine the improvement in the compliance assessment in clinical trials • Address the issues and challenges in the compliance • Identify the resources and tools available to increase compliance

2. Who Will Benefit: • This topic applies to personnel / companies doing research or involved in the clinical trials. The following will benefit most include: • Principle Investigators(PIs) • Study Coordinators • Nurses • Senior Clinical Research Associates(CRAs) • Clinical Research Project Manager • Contract Research Organizations (CROs) • Clinical Research Coordinators SpeakerProfile: Dr. NaginaParmar is a certified clinical research professional and senior clinical research Associate. Dr. Parmar is involved in coordinating various phase II -IV national and international clinical trials. She is also involved in developing SOPs (Standard operating Procedures) and research elements database in the hematology oncology department. Dr. Parmar is teaching Biology, Microbiology, Life Sciences for Clinical practice, Principles of clinical research to undergraduate and graduate courses at Ryerson University. She has published more than 30 journal articles and reviews in various national and international journals and SOCRA source. Dr. Parmar is an active member of the Society of Clinical Research Associates (SoCRA) and Networks of Networks (N2). Dr. Parmar has given various career development seminars at University of Toronto to graduates and postgraduates, webinars and trainings and is actively involved in reviewing textbooks for Pearson education Canada and John Wiley and Sons. Toregister visit this webinar https://compliancetrainings.com/siteengine/Login.aspx