Webinar On Patient Compliance in Drug Trials

MessageThis Webinar is over
Date Aug 7, 2014
Time 1 PM
Cost $249.00
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. Therefore it is necessary and pertinent to explore the resources that are available for researchers to increase the compliance in their populations of patients who are participating in the clinical trials.
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
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
Senior Clinical Research Associates(CRAs)
Clinical Research Project Manager
Contract Research Organizations (CROs)
Clinical Research Coordinators
Price Tags:
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
Speaker Profile
Dr. Nagina Parmar 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.
For more information contact
Compliance Trainings
5939 Candlebrook Ct, 
Mississauga, ON L5V 2V5, 
Customer Support : 416-915-4458 
Email : support@compliancetrainings.com


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