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Course name Direct-to-Consumer Pharmacogenomic Testing

On-demand

Self-paced

1 hour (online)

Free

This online, self-paced, text-based module educates healthcare professionals towards a better understanding of the benefits and limitations of direct-to-consumer pharmacogenomic testing, when to pursue confirmatory clinical testing, and how to interpret pharmacogenomic test results using evidence-based resources.

It was developed by the National Human Genome Research Institute (NHGRI) Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG).

To access, log in to our site (to right of this page; free registration) and click 'continue' to enroll (it's free!).

Faculty

Planning Committee for the ISCC-PEG Pharmacogenomics Learning Series:

Philip Empey, PharmD, PhD, FCCP (University of Pittsburgh School of Pharmacy)
Andrew Monte, MD, PhD (University of Colorado)
Trina Walker, DNP, APRN, FNP-C (Creighton University)
Nguyen Park, MS, PA-C (National Human Genome Research Institute)
Jeneva Gularte-Rinaldo, PhD, RN (Samuel Merritt University)

Course Directors

Roseann S. Donnelly (Gammal), PharmD, BCPS
Associate Professor
Massachusetts College of Pharmacy and Health Sciences

Additional Content Reviewers

Cyrine-Eliana Haidar, PharmD, BCPS, BCOP, FASHP, Clinical Pharmacogenetics Coordinator, St. Jude Children’s Research Hospital
David Kisor, PharmD, FCP, Professor of Pharmaceutical Sciences and Pharmacogenomics, Manchester University

Course details

TARGET AUDIENCE

All healthcare professionals

LEARNING OBJECTIVES

Upon completion of this activity, participants should be able to:

Differentiate between the delivery models for pharmacogenomic testing.
Identify the benefits and limitations of direct-to-consumer (DTC) pharmacogenomic testing.
Interpret DTC pharmacogenomic test results.
Evaluate the clinical actionability of genetic variants detected by a DTC pharmacogenomic test using evidence-based resources.
Determine when confirmatory clinical testing is needed when faced with DTC pharmacogenomic test results.
Explain why confirmatory clinical pharmacogenomic test results may differ from direct-to-consumer pharmacogenomic test results for the same patient.
Discuss issues related to documenting DTC pharmacogenomic test results in the electronic health record.

NHGRI ISCC-PEG

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Course name The Economics of Pharmacogenomic Testing

On-demand

Self-paced

0.5 hour (online)

Free

This online, self-paced, text-based module educates healthcare professionals towards a better understanding of the benefits and limitations of direct-to-consumer pharmacogenomic testing, when to pursue confirmatory clinical testing, and how to interpret pharmacogenomic test results using evidence-based resources.

It was developed by the National Human Genome Research Institute (NHGRI) Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG).

To access, log in to our site (to right of this page; free registration) and click 'continue' to enroll (it's free!).

Faculty

Planning Committee for the ISCC-PEG Pharmacogenomics Learning Series:

Philip Empey, PharmD, PhD, FCCP (University of Pittsburgh School of Pharmacy)
Andrew Monte, MD, PhD (University of Colorado)
Trina Walker, DNP, APRN, FNP-C (Creighton University)
Nguyen Park, MS, PA-C (National Human Genome Research Institute)
Jeneva Gularte-Rinaldo, PhD, RN (Samuel Merritt University)

Course Directors

Karen Niemchick, PhD, MHS
Grand Valley State University

Additional Content Reviewers

Joshua Peterson, MD, Vanderbilt University
Caleb Bupp, MD, Spectrum Health

Course details

TARGET AUDIENCE

All healthcare professionals

LEARNING OBJECTIVES

Upon completion of this activity, participants should be able to:

Understand a basic cost analysis
Compare benefits of genetic testing with traditional treatment.
Gain experience in accessing genetic test information.

NHGRI ISCC-PEG

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Course name Navigating Pharmacogenomic Testing Coverage in Medicare Populations

On-demand

Self-paced

1 hour (online)

Free

This online, self-paced, text-based module educates healthcare professionals towards a better understanding of the benefits and limitations of direct-to-consumer pharmacogenomic testing, when to pursue confirmatory clinical testing, and how to interpret pharmacogenomic test results using evidence-based resources.

It was developed by the National Human Genome Research Institute (NHGRI) Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG).

To access, log in to our site (to right of this page; free registration) and click 'continue' to enroll (it's free!).

Faculty

Planning Committee for the ISCC-PEG Pharmacogenomics Learning Series:

Philip Empey, PharmD, PhD, FCCP (University of Pittsburgh School of Pharmacy)
Andrew Monte, MD, PhD (University of Colorado)
Trina Walker, DNP, APRN, FNP-C (Creighton University)
Nguyen Park, MS, PA-C (National Human Genome Research Institute)
Jeneva Gularte-Rinaldo, PhD, RN (Samuel Merritt University)

Course Directors

	Sara Rogers, PharmD, BCPS American Society of Pharmacovigilance Texas A&M University
	Benjamin Brown American Society of Pharmacovigilance
	Christine Formea, PharmD, BCPS, FCCP, FASHP Children’s Hospital Colorado

Additional Content Reviewers

Jai Patel, PharmD, BCOP, CPP, Levine Cancer Institute, Atrium Health
Chet Robson, DO, MHCDS, FAAFP, Jasper Health

Course details

TARGET AUDIENCE

All healthcare professionals

LEARNING OBJECTIVES

Upon completion of this activity, participants should be able to:

Define relevant reimbursement related terminology
Review key components of payer coverage guidance for pharmacogenomics testing
Describe technical requirements for test reports
Understand special documentation requirements to show medical necessity

NHGRI ISCC-PEG

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Course name Test2Learn PGx Certificate Program - Harding 2025

Fall 2025

Private Training

This 20-hour competency-based education program enables learners to apply and implement pharmacogenomics in practice by using real genetic data in highly-interactive exercises. It is comprised of 16 hours of self-paced, online modules that unlock automatically with course progression and 4 hours of live training led by experts that will challenge you to use the concepts learned in real-life scenarios. Upon completion, a certificate, a microcredential (badge), and continuing education can be awarded.

To enroll in this course, log in to our site (top right of this page; free registration) and then return to the bottom of this page to self-enroll. You will be granted immediate access to start your training.

FACULTY EXPERTS TEACHING THE LIVE PROGRAM

	Philip E. Empey, PharmD, PhD, FCCP Associate Director, Institute of Precision Medicine; Associate Professor, Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy Faculty profile		James Coons, PharmD, FCCP, FACC, BCCP PGY2 Cardiology Residency Program Director, Professor, Pharmacy and Therapeutics, School of Pharmacy, University of Pittsburgh Faculty profile
	Lucas Berenbrok, PharmD, MS, BCACP, TTS Associate Professor, Pharmacy and Therapeutics School of Pharmacy, University of Pittsburgh Faculty profile

COURSE SCHEDULE

Self-paced, online study
Available immediately upon registration; to be completed in advance of the live program date.

Faculty-led, live session
Live portion of this program will be led by Dr. Landry Kamdem

ADDITIONAL COURSE DETAILS

Target audience, education modules, and learning objectives

TARGET AUDIENCE

All healthcare professionals

EDUCATION MODULES

Self-paced, online study

Precision medicine and PGx (2 units)
Foundations of PGx (4 units)
PGx testing (3 units)
PGx decision making (6 units)
PGx in clinical practice (5 units)
Keys to successful implementation (7 units)

Live session

Variation: One size does not fit all
Using of trustworthy online information
How does a lab assign diplotypes
Phenotypes to recommendations
Decision making in practice: working through complex cases
Developing PGx patient care plans
Advancing your successful implementation and Wrap Up

LEARNING OBJECTIVES

Upon completion of this activity, participants should be able to:

Foundational
Genetics
Concepts (FG)

Explain basic genetics concepts using appropriate nomenclature.
Recognize the combined impact of genetic, behavioral, social, and environmental factors in the manifestation of disease and drug response.
Identify drug- and disease-associated genetic variations that facilitate development of prevention, diagnostic, and treatment strategies.
Differentiate between the clinical diagnosis of disease informed by genetics and the identification of genetic predisposition to disease.
Assess differences in genetic testing technologies, including sequencing and genotyping.
Recognize the legal protections against discrimination based on genetic test results.

Clinical PGx
(CP)

Identify pharmacogenomic test results that are relevant to a patient’s care.
Interpret pharmacogenomic test results, including translating genotype to phenotype to drug therapy recommendation.
Determine the impact of genetic variation on pharmacokinetics and/or pharmacodynamics.
Identify medication-related problems that may be related to genetic variability, even when a pharmacogenomic test has not been done.
Recognize disease implications of pharmacogenomic test results and refer the patient to a genetics-trained healthcare provider when necessary.
Use family history to assess predisposition to disease and drug response.
Assess the quality and source of existing pharmacogenomic test results.
Distinguish between actionable and non-actionable pharmacogenomic test results using high-quality, evidence-based pharmacogenomics databases and clinical guidelines.
Integrate pharmacogenomic test results with other clinical variables to optimize medication therapy.
Recommend pharmacogenomic testing when appropriate.
Consider the cost, cost-effectiveness, and reimbursement issues relevant to pharmacogenomic tests and services.
Implement a pharmacogenomics-guided care plan in collaboration with the patient, caregivers, and other health professionals.
Document pharmacogenomic test results in the electronic health record.
Follow-up and monitor a pharmacogenomics-guided care plan.
Collaborate as a member of an interprofessional clinical pharmacogenomics team.
Identify patient populations that may be most likely to benefit from pharmacogenomic testing.
Identify genetic variations that predispose patients to adverse drug reactions and modify therapy accordingly to mitigate the risk.
Recognize the differences in pharmacogenomic allele frequencies among ancestry groups to guide appropriate test selection and maximize the appropriate use of medications in a population.
Educate patients and professional colleagues on the benefits and limitations of pharmacogenomics to optimize drug therapy.
Use a culturally-sensitive approach that considers potential ethical concerns when counseling patients about pharmacogenomic test results.
Use evidence-based resources and pharmacogenomics information to advance patient care.
Oversee clinical pharmacogenomics operations.
Fulfill a medication order considering the clinical implications of pharmacogenomics.
Create a written plan for continuous professional development in clinical pharmacogenomics.

DISCLAIMER STATEMENT

The information presented at this activity represents the views and opinions of the individual presenters, and does not constitute the opinion or endorsement of, or promotion by, the UPMC Center for Continuing Education in the Health Sciences, UPMC / University of Pittsburgh Medical Center or Affiliates and University of Pittsburgh School of Medicine. Reasonable efforts have been taken intending for educational subject matter to be presented in a balanced, unbiased fashion and in compliance with regulatory requirements. However, each program attendee must always use his/her own personal and professional judgment when considering further application of this information, particularly as it may relate to patient diagnostic or treatment decisions including, without limitation, FDA-approved uses and any off-label uses.

Meet planning committee and course faculty

PLANNING COMMITTEE

	Philip Empey, PharmD, PhD, FCCP Associate Professor, Pharmacy and Therapeutics, Associate Director, Institute of Precision Medicine; University of Pittsburgh School of Pharmacy (Course Director)
	James Coons, PharmD, FCCP, FACC, BCCP Professor, Pharmacy and Therapeutics, PGY2 Cardiology Residency Program Director, University of Pittsburgh School of Pharmacy
	Lucas Berenbrok, PharmD, MS, BCACP, TTS Associate Professor, Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy
	Ashley Stewart, EdD, MA Instructional Designer, University of Pittsburgh School of Pharmacy
	Deepak Voora, MD Executive Director, VA National Pharmacogenomics Program VA Central Office, Washington, DC
	Jill Bates PharmD, MS, BCOP, DipACLM, FASHP Deputy Executive Director, VA National Pharmacogenomics Program VA Central Office, Washington, DC
	Trina Walker, DNP, APRN, FNP-C Assistant Professor, Nursing Creighton University
	Nguyen Park, MS, PA-C President and Founder, Society of PAs in Genetics/Genomics

PRENSENTERS (ALPHABETICAL ORDER)

	Lucas Berenbrok, PharmD, MS, BCACP, TTS Associate Professor, Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy
	Kelly Caudle, PharmD, PhD, BCPS, FCCP Associate Member, St. Jude Children's Research Hospital CPIC Director
	James Coons, PharmD, FCCP, FACC, BCCP Professor, Pharmacy and Therapeutics, PGY2 Cardiology Residency Program Director, University of Pittsburgh School of Pharmacy
	Philip Empey, PharmD, PhD, FCCP Associate Professor, Pharmacy and Therapeutics, Associate Director, Institute of Precision Medicine; University of Pittsburgh School of Pharmacy
	Mylynda Massart, MD, PhD Associate Professor, Department of Family Medicine Primary Care Precision Medicine University of Pittsburgh
	Lisa Parker, PhD Director, Center for Bioethics and Health Law University of Pittsburgh
	Katherine Robinson, PharmD, MS, BCPS Clinical Pharmacogenomics Pharmacist University of Pittsburgh School of Pharmacy
	Sara Rogers, PharmD Clinical Assistant Professor Texas A&M University
	Kayla Rowe, PharmD Clinical Pharmacogenomics Fellow University of Pittsburgh
	Robert Schuck, PharmD, PhD Deputy Director, Division of Translational and Precision Medicine Office of Clinical Pharmacology Center for Drug Evaluation and Research US Food and Drug Administration
	Todd Skaar, MS, PhD Professor, Clinical Pharmacology Indiana University School of Medicine
	James Stevenson, PharmD, MS Assistant Professor, Departments of Medicine and Pharmacology & Molecular Sciences Johns Hopkins University School of Medicine
	Emma Tillman, PharmD, PhD Associate Research Professor, Division of Clinical Pharmacology Indiana University School of Medicine
	Michelle Whirl-Carrillo, PhD Principal Investigator and Director, PharmGKB Department of Biomedical Data Science Stanford University

CONFLICT OF INTEREST

No members of the planning committee, speakers, presenters, authors, content reviewers and/or anyone else in a position to control the content of this education activity have relevant financial relationships with any entity producing, marketing, re-selling, or distributing health care goods or services, used on, or consumed by, patients to disclose.

HOW TO OBTAIN CONTINUING EDUCATION

Continuing education can be claimed for the above learner groups. Learners must complete the full program (all modules, attain grades of 80% or higher on assessments, and participate in the live session) as well as submit the required information to the CE office (e.g. profile information and evaluations) prior to the deadline to receive continuing education credit. Partial credit will not be awarded.

Harding University

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