Continuing Education Credits
At the conclusion of this meeting, participants should be able to:
- Discuss challenges for ensuring compliance to meet regional requirements
- Examine process optimization when collaborating with CROs and Cloud computing across the lifecycle continuum
- Outline the importance of maximizing content reuse, metadata, aligning standards, and technology with the process
- Describe organizational processes and governance to ensure integrity, quality, and security of records
- Explain current global regulatory agency requirements and future initiatives
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; +1.703.506.3275.
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 up to 1.7 CEUs for this program and tutorial, if applicable. Participants must attend the entire program in order to be able to receive an IACET statement of credit. No partial credit will be awarded.
If you would like to receive a statement of credit, you must attend the program (and tutorial, if applicable), scan your badge once a day, and complete the on-line credit request process through My Transcript. To access My Transcript, please go to www.diahome.org, select “Login to My DIA” and you will be prompted for your user ID and password. Select “My Transcript” (left side bar) and “Credit Request” to process your credit request. 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 on Thursday, October 31, 2013.
This conference is part of DIA’s Certificate Program and is awarded the following:
For more information go to www.diahome.org/certificateprograms
CONTINUING EDUCTION CREDIT ALLOCATION
- Project Management Certificate Program: 8 Elective Units
- Regulatory Affairs Certificate Program: 10 Elective Units
Tutorial 1: eCSRs: .3 IACET CEUs
Tutorial 2: Get Ready for Global ISO IDMP, Including Lessons Learned From the EU XEVMPD: .3 IACET CEUs
Conference: EDM and ERS/eCTD: Impact of e-Initiatives on Content and Context: 1.4 IACET CEUs
It is Drug Information Association 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. Faculty disclosures will be included in the course materials.
Unless otherwise disclosed, DIA acknowledges that the statements made by speakers are their own opinion and not necessarily that of the organization they represent, or that of the Drug Information Association. Speakers, agenda, and CE information are subject to change without notice.
Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.
View DIA’s Grievance Policy.
AMERICANS WITH DISABILITIES ACT (ADA)
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.