Webinar On Patient Compliance in Drug Trials

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Webinar
On Patient Compliance in Drug Trials
Product Id
Product Id
Product Id
FDB1321
Category
Food, Drugs Biologics
Category
Food, Drugs Biologics
Category
Scheduled On
Scheduled On
Food, Drugs Biologics
Scheduled On
Thursday, July 17, 2014 at 1300 Hrs
Scheduled On
Monday, June 16, 2014 at 1300 Hrs
Scheduled On
Duration
Duration
Thursday, July 17, 2014 at 1300 Hrs
Duration
60 Minutes
Duration
60 Minutes
Speaker
Dr. Nagina Parmar
To register for this webinar visit our
https//compliancetrainings.com/SiteEngine/Product
DetailView.aspx?idFDB1321
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 dont 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,
investigators, pharmacist and Physicians 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

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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

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.

To register visit this webinar https//compliancet
rainings.com/siteengine/Login.aspx