Webinar On Patient Compliance in Drug Trials

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

Nurses

Senior Clinical Research Associates(CRAs)

Clinical Research Project Manager

Contract Research Organizations (CROs)

Clinical Research Coordinators

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299