A
well-designed Data Management Plan (DMP) provides a detailed description of how
to handle data under any foreseeable circumstances and establishes processes
for how to deal with unplanned issues. The DMP is study specific, is considered
a “living document,” and is subject to audit; therefore, it is important to
understand the content requirements and rationale for its creation.
In this web seminar, we
will focus on the importance of the creation of a DMP and the expected content
that this document should contain. Attendees will be provided with a sample
template for review.
- Identify the rationale for creation of a robust
DMP
- Describe the documentation required
for a DMP when utilizing both paper and Electronic Data Capture (EDC)
applications
- List the components of a DMP as
defined in the Society for Clinical Data Management (SCDM) Good Clinical
Data Management Practices (GCDMP) document
- Apply standards for creating,
approving, and maintaining DMPs
- Clinical Data Managers
- Project Managers
- Clinical Research Personneltem 1
Denise
G. Redkar-Brown, MT
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biographies
$735
Includes up to 20
participants at one site. All participants (up to 20) are eligible for
“Certificates of Attendance,” and accreditation, provided that accreditation
requirements are met. For groups larger than 20 or for additional sites, please
call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Barnett International is accredited by the
Accreditation Council for Pharmacy Education as a provider of continuing
pharmacy education. Participants will
receive 1.5 hours (0.15 CEUs) of continuing education credit for full
participation, including the completion of a pre-test, post-test, and program
evaluation. Barnett International will
issue a receipt of completion for earned CEUs within three weeks of program
completion. ACPE#: 0778-0000-17-025-L01-P.
Released: 5/17.
Hold
this course at your company! For more information, contact Naila Ganatra at +1
215.413.2471.