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Mandarin Oriental Washington D.C.

Jan 25, 2016 8:30 AM - Jan 27, 2016 3:00 PM

1330 Maryland Avenue, SW, Washington, DC 20024

Pharmacovigilance and Risk Management Strategies 2016

Discuss opportunities, challenges, and practical aspects of managing risk in the context of benefits, for medical product safety and pharmacovigilance.

Continuing-Education

ACPEDIA is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. This program is designated for up to 20 contact hours or 2.0 continuing education units (CEU’s).

ACPE Credit Requests MUST BE SUBMITTED by Friday, March 11, 2016. 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. Obtain your NABP e-Profile.

PIMThis activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of Postgraduate Institute for Medicine (PIM) and DIA. PIM is accredited by the ACCME to provide continuing medical education for physicians.

PIM designates this live activity for a maximum of 16.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.


ANCCCorexcel is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.

Corexcel designates this activity for a maximum of 23 contact hours.


IACETDIA has been accredited as an Authorized Provider by the International Association for Continuing Education and Training (IACET).

As an IACET Authorized Provider, DIA offers CEUs for its programs that qualify under the ANSI/IACET Standard. DIA is authorized by IACET to offer up to 2.3 CEUs for this program. Participants must attend the entire program (and tutorial(s) if applicable) in order to be able to receive an IACET statement of credit. No partial credit will be awarded.


View Continuing Education Credit Allocation

DIA’s Certificate Program Statement

This program is part of DIA’s Certificate Program and is awarded the following:
  • Clinical Research Certificate Program: 12 Elective Units
  • Clinical Safety and Pharmacovigilance Certificate Program: 4 Elective Units
  • Regulatory Affairs Certificate Program: 12 Elective Units
Learn More
The Postgraduate Institute for Medicine (PIM) and DIA require instructors, planners, managers and other individuals who are in a position to control the content of this activity to disclose any real or apparent conflict of interest they may have as related to the content of this activity. All identified conflicts of interest are thoroughly vetted by PIM and DIA for fair balance, scientific objectivity of studies mentioned in the materials or used as the basis for content, and appropriateness of patient care recommendations.
NameCredit TypeMax CreditsCEU
Pharmacovigilance and Risk Management Strategies 2Credit TypeACPEMax Credits13.50CEU1.350
Pharmacovigilance and Risk Management Strategies 2Credit TypeCMEMax Credits16.50CEU0.000
Pharmacovigilance and Risk Management Strategies 2Credit TypeIACETMax Credits16.50CEU1.700
Pharmacovigilance and Risk Management Strategies 2Credit TypeRNMax Credits16.50CEU0.000
Tutorial #1 - Pharmacovigilance and Risk ManagemenCredit TypeACPEMax Credits5.75CEU0.575
Tutorial #1 - Pharmacovigilance and Risk ManagemenCredit TypeIACETMax Credits5.75CEU0.600
Tutorial #1 - Pharmacovigilance and Risk ManagemenCredit TypeRNMax Credits5.75CEU0.000
Tutorial #2 – FDA Adverse Event Reporting SystemCredit TypeACPEMax Credits3.25CEU0.325
Tutorial #2 – FDA Adverse Event Reporting SystemCredit TypeIACETMax Credits3.25CEU0.300
Tutorial #2 – FDA Adverse Event Reporting SystemCredit TypeRNMax Credits3.25CEU0.000
Tutorial #3 – Periodic Benefit-Risk Evaluation RepCredit TypeIACETMax Credits3.25CEU0.300
Tutorial #3 – Periodic Benefit-Risk Evaluation RepCredit TypeRNMax Credits3.25CEU0.000
Tutorial #4 – Principles and Practice of PharmacovCredit TypeACPEMax Credits3.25CEU0.325
Tutorial #4 – Principles and Practice of PharmacovCredit TypeIACETMax Credits3.25CEU0.300
Tutorial #4 – Principles and Practice of PharmacovCredit TypeRNMax Credits3.25CEU0.000

Statement of Credit:

If you would like to receive a statement of credit, you must attend the conference (and tutorial(s), if applicable), sign in at the registration desk each morning, and complete the online credit request process through My Transcript. My Transcript will be available for credit requests beginning Wednesday, February 10, 2016. To access My Transcript:

  • Visit DIAglobal.org, select “Sign in” and you will be prompted for your user ID and password
  • Choose MENU, found in the upper left corner
  • Under CONFERENCES select “Continuing Education"
  • Select the blue “My Transcript” button followed by “Credit Request” to process your credit request for the conference (and/or tutorials, if applicable).
The evaluation closes on Wednesday, February 17, 2016.

To view DIA’s Grievance Policy, visit DIAglobal.org/CE.

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