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Good Clinical Practices for the Clinical Research Professional

May 29 2013 12:00PM - Jun 6 2013 2:00PM | Online

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Overview 

Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies.

Featured Topics 

  • Roles and responsibilities of each member of the study team
  • Regulations and guidelines that govern clinical investigations
  • Informed consent elements and processes
  • Successful patient recruitment and retention strategies
  • Adverse event handling and reporting
  • Preparing for audits and audit process

Who Should Attend 

  • Clinical investigators
  • Clinical research professionals
  • Sub-investigators
  • Study staff

Learning Objectives 

At the conclusion of this activity, participants should be able to:

  • Identify the roles and responsibilities of each member of the study team, including the clinical investigator, sub-investigator, study staff, IRB, and sponsor
  • Apply the regulations and guidelines for conducting safe and effective clinical trials
  • Describe the various processes for informed consent
  • Describe the requirements in reporting adverse events

Special Offers 

Register More than One Group Site and Save 15%!

Contact Information 

Registration Questions
Elizabeth Espich, Customer Service Associate
Phone +1.215.442.5802
Fax +1-215.442.6199
Elizabeth.Espich@diahome.org

Agenda and Event Logistics
Colleen Buckley, Event Planner
Phone +1.215.442.6108
Fax +1.215.442.6199
Colleen.Buckley@diahome.org

Technical Requirements 

Click here for minimum system requirements.

Faculty 

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Continuing Education 

ACPE Credit Request Update
DIA is required by the Accreditation Council for Pharmacy Education (ACPE) to report pharmacy-requested CEUs through the CPE Monitor system. All ACPE-certified activity credit requests need to be submitted through DIA’s My Transcript within 45-days post activity. Pharmacists will need to provide their National Association of Boards of Pharmacy (NABP) e-Profile ID and date of birth (MMDD) to ensure the data is submitted to the ACPE and NABP properly. If you need to obtain your NABP e-Profile, please visit www.cpemonitor.net.

The Drug Information Association is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. The Drug Information Association designates this educational activity for up to 8 contact hours or .8 CEUs. Type of Activity: Knowledge ACPE: A UAN and designated credit amount is assigned below for each part in the online training course:
Part 1: 0286-0000-13-016-L04-P, 2 contact hours or .2 CEUs:
Part 2: 0286-0000-13-017-L04-P, 2 contact hours or .2 CEUs:
Part 3: 0286-0000-13-018-L04-P, 2 contact hours or .2 CEUs:
Part 4: 0286-0000-13-019-L04-P, 2 contact hours or .2 CEUs

Drug Information Association has been accredited as an Authorized Provider by the International Association for Continuing Education and Training (IACET), 1760 Old Meadow Road, Suite 500, McLean, VA 22102.

As an IACET Authorized Provider, Drug Information Association offers CEUs for its programs that qualify under the ANSI/IACET Standard. Drug Information Association is authorized by IACET to offer .8 CEUs for this program. Participants must attend the entire program in order to be able to receive an IACET statement of credit. No partial credit will be awarded.

This program is part of DIA’s Certificate Program and is awarded the following:
• Clinical Research Certificate Program: 4 Core Units

For more information go to www.diahome.org/certificateprograms

Name Credit Type Max Credits CEU
Good Clinical Practices for the Clinical Research ACPE 8.00 0.800
Good Clinical Practices for the Clinical Research IACET 8.00 0.800

Disclosure Policy:

It is DIA policy that anyone in a position to control the content of a continuing education activity must disclose to the program audience (1) any real or apparent conflict(s) of interest related to the content of their presentation and/or the educational activity, and (2) discussions of unlabeled or unapproved uses of drugs or medical devices. Disclosure statements will be included in the course materials.

Statement of Credit:

Continuing education credits are available to learners who participate in the live online training activity. Participants must attend the live online training activity in order to be eligible to receive a statement of credit. To request credit, complete the online credit request process through My Transcript at www.diahome.org. Participants will be able to download a statement of credit upon successful submission of the credit request. My Transcript will be available for credit requests two weeks after the last day of the activity.

Continuing education credits are not available for participation in the archived sessions of the online training activity.

To view DIA’s Grievance Policy, please visit the CE page on the DIA website at www.diahome.org/CE

Agenda  

Day 1 Wednesday, May 29, 2013

  • 12:00PM - 2:00PM

    Part 1: Regulations and Guidelines that Govern Clinical Investigations

Day 2 Thursday, May 30, 2013

  • 12:00PM - 2:00PM

    Part 2: Drug Development Process

Day 3 Wednesday, June 05, 2013

  • 12:00PM - 2:00PM

    Part 3: Practices that Ensure Effective and Efficient Study Conduct

Day 4 Thursday, June 06, 2013

  • 12:00PM - 2:00PM

    Part 4: Practices that Ensure Effective and Efficient Study Conduct (continued)

Registration Fees 

Other Fees

Group Site
$2250.00

Member

Charitable Nonprofit/Academia Member Individual
$450.00
Member Government Individual
$450.00
Member Standard Individual
$895.00

Non-Member

Charitable Nonprofit/Academia Nonmember Individual
$535.00
NonMember Government Individual
$535.00
NonMember Standard Individual
$985.00
Group Discounts

GROUP SITE:
Group Site is a license for one internet and audio log-in, allowing multiple viewers at one physical location. All other fees are for one log-in allowing one viewer.

*Receive a 15% discount on the entire purchase when you register for more than one group site at the same time. Valid only when group sites are purchased online for this training series.

This online training offering is sold as one complete series and cannot be purchased in parts.


Cancellation Policy: No refunds will be provided in the event of a participant’s cancellation since all costs for this online training course have been prepaid by DIA. DIA reserves the right to modify or cancel programs and/or substitute presenters or panelists. DIA is not responsible for failure to deliver programs due to circumstances beyond its control.

Participants with Disabilities: Reasonable accommodations will be made available to persons with disabilities who attend an educational activity. Contact the DIA office in writing at least 15 days prior to event to indicate your needs.

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