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Thursday, January 11

U.S. Pharmaceutical Market: Trends, Issues, and Outlook

Doug Long, M.B.A., VP, Industry Relations, IQVIA

Doug will provide market perspective on pharmacy and pharmaceutical industry trends, issues, and forecasts for 2024 and beyond.

Practical AI in the Pharmacist Workflow

David Sellars, Principal, Product Innovations, DrFirst

Artificial intelligence (AI) isn’t just a buzzword. It’s no longer a false promise. Today there are pharmacies in the United States and Canada using practical, powerful AI to automate data entry workflows. AI-augmented workflows are faster and safer. In this session, David will show how AI is used in retail pharmacy workflows to manage free text allergies, sigs, and advanced drug matching, and even to convert faxes into retail pharmacy orders in real time.

DSCSA Compliance Requirements Regulatory and Industry Status Report

Randy Hoggle, B.Pharm., D.Ph., M.B.A., Managing Director, Advasur

Randy’s presentation will bring you up to date on the Drug Supply Chain Security Act (DSCSA). He will cover topics including: the current DSCSA federal regulatory compliance enforced requirements status, as well as the remaining and additional requirements status; supply chain capabilities and authorized trading partner (ATP) remaining issues to address; supply chain planned capabilities to meet these subsequently released/policed requirements and the resulting effort required by type of ATP; and residual issues and the regulatory, staffing, and financial impact on the ATP community to date and over the next three to five years.

PDMPs and ASAP 5.0 Updates

Kevin Borcher, Pharm.D., Senior Project Coordinator, Institute for Intergovernmental Research (IIR)/PDMP TTAC

The ASAP PDMP (prescription drug monitoring program) standard has not been updated since 2019. Since then, PDMPs have progressed and evolved into systems to improve patient safety. Kevin will cover how ASAP worked with multiple stakeholders, including vendors and PDMP administrators, to develop the most significant upgrade to the standards in years.

Opportunities for Pharmacy Practice Transformation and Creating an IMPACT in Population Health

Ben Bluml, B.S.Pharm., Executive Director and SVP, Research and Innovation, APhA Foundation

Ben will discuss the APhA Foundation’s portfolio of active research and innovation initiatives focused on patient-centered, team-based care that includes pharmacists. Two of these active initiatives are credentialing and compensating pharmacists just like their physician colleagues on the healthcare team. Creating new opportunities for pharmacist service delivery payments that enable pharmacists to address population health needs and social determinants of health (SDOH) are hallmarks of several others. Most interestingly, though, will be details about the dedicated work in diabetes prevention that continues under the APhA Foundation’s CDC-recognized Umbrella Hub Arrangement (UHA) status that allows pharmacists to be compensated for providing Medicare National Diabetes Prevention Program (National DPP) services.

Friday, January 12

What’s Driving Healthcare Team Evolution

Ken Whittemore, Pharm.D., VP Pharmacy and Regulatory Affairs, Surescripts

Ken will delve into the transformation happening in pharmacy-provided healthcare. What milestones have brought us to the care being provided today, and what is on the horizon? Explore how technology, legislative changes, and patient-driven motivations are helping to reshape the services pharmacies provide.

Error-free Data: Yes, Please!

Brandi Van Patton, Pharm.D., Chief Clinical Officer, LogiCoy

Data quality is at the heart of data collection. Knowing data is complete and error-free can enhance patient care. However, there are many components to data quality that can be difficult to meet. Brandi will address the solutions that are needed to assist healthcare providers to not only comply with standards, but meet a high level of data quality as well.

Medicare Payments and Beneficiary Smoothing: What Pharmacies Need to Know

Ann Johnson, President, Pharmacy Healthcare Solutions

Ann will present an overview of the Inflation Reduction Act’s “price smoothing” provision, which is anticipated to begin in 2025. She will cover implications for patients, payers, and pharmacies, focusing on the software system changes necessary to implement this.

340B Trends and Issues: Is It Time for Reform?

Marsha Millonig, M.B.A., B.Pharm., President and CEO, Catalyst Enterprises

The federal 340B drug pricing program requires manufacturers to extend lower, discounted prices for outpatient drugs to eligible providers, called “covered entities,” in order to have their products covered under Medicaid and the Medicare Part B programs. The covered entities that receive the 340B discounts for covered outpatient drugs are providers who care for patients who are underinsured and uninsured, or otherwise vulnerable. The goal was “to stretch scarce federal resources as far as possible, reaching more eligible patients and providing more comprehensive services.”

Since it was created, the list of eligible providers has expanded, the number of providers participating in the program has increased, and the total dollars of discounted drugs purchased through the 340B program has grown. There are currently concerns about provider compliance with the 340B program’s rules, and whether there is enough oversight of participants to address duplicate discounts or discounted products going to patients who are not eligible.

In this session, Marsha will bring you the latest trends in 340B and outline the major issues that have been raised. She will also talk about the latest efforts at reforming the program.

Speaker Bios

Doug Long

Doug Long, M.B.A., is vice president of industry relations at IQVIA, one the world’s largest pharmaceutical information companies. IQVIA offers services to the pharmaceutical industry in over 101 countries around the globe.

Doug’s fundamental task is to help secure data for all existing and new databases supported by IQVIA, manage supplier, manufacturer and association relationships, and develop information for data partners. As a direct consequence of his involvement in these areas, Doug has considerable experience with, and a unique perspective on, the changing U.S. and global healthcare marketplace and pharmaceutical supply chain.

Doug received a B.A. degree from DePauw University and an M.B.A. in management from Fairleigh Dickinson University.

David Sellars

David Sellars, CEng, is principal, product innovations at DrFirst. He has over 20 years of healthcare experience with a deep emphasis in big data, artificial intelligence, healthcare interoperability, programming, and systems optimization. He has served at DrFirst since 2010, leading R&D for the Product Team and holds multiple AI patents applied to healthcare. These efforts have received multiple innovation and safety awards from the industry and partners alike. His experience in healthcare started with the five top EHR’s, including implementing clinical modules and large multi-hospital migrations and more recently has been focused on the retail pharmacy space.

Randy Hoggle

J. Randle Hoggle, B.Pharm., D.Ph., M.B.A., is managing director of Advasur, which provides the Advasur 360 DSCSA Compliance Turn-Key Outsource System and Services for the dispenser market. Randy has over 35 years of experience in the pharmaceutical supply chain management Industry.

Since 2000, Randy has founded four companies that have built four systems for the federal government with the last system being the FDA CDER Electronic Labeling Information Processing System (ELIPS), completed in 2013 as the DSQA act was passed. More recently, FDA licensed the Advasur 360 system for selected contractors to use in two studies that assessed the ability of small dispensers to comply with DSQA. Both were successfully completed with 100% compliance by the 47 small dispenser participants.

Randy received his D.Ph. degree from the University of Oklahoma and his M.B.A. from Duke University.

Ben Bluml

Benjamin Bluml, B.S.Pharm., is the executive director and senior vice president for research and innovation at the American Pharmacists Association (APhA) Foundation. Along with his 27-plus years as the principal architect for the clinical and technology models in the Foundation’s patient care programs and 12 years of pharmacy practice experience, Ben is the author of numerous innovative health care software applications and professional journal publications related to his work on collaborative practice, health information technology, interdisciplinary patient care, and quality improvement.

He works with pharmacists, physicians, payers, technology companies, research and public health organizations across the United States to design and implement innovative patient-centered, team-based care programs and health care service delivery systems.

Bluml received his B.S.Pharm. from the University of Missouri Kansas City School of Pharmacy. 

Kevin Borcher

Kevin Borcher, Pharm.D., is the senior project coordinator for the Prescription Drug Monitoring Program (PDMP) Training and Technical Assistance Center at the Institute for Intergovernmental Research. Kevin is responsible for developing and delivering programmatic and technical assistance for thePDMP and other justice and public health initiatives.

Prior to this, Kevin was the pharmacy informatics coordinator at Nebraska Methodist Hospital and most recently was the vice president of PDMP and pharmacy programs for Nebraska at CyncHealth.

Kevin  has worked within areas involving geriatrics, behavioral health, and informatics. He has served on the Nebraska Board of Pharmacy for over ten years and on the Nebraska Board of Health for over six years.

He received his Pharm.D. from the University of Nebraska Medical Center and completed a residency in Phoenix, Ariz.

Ken Whittemore

Ken Whittemore, Pharm.D., is VP of pharmacy and regulatory affairs at Surescripts, the nation’s largest health information network. Pharmacies, payers, pharmacy benefit managers (PBMs), physicians, hospitals, health information exchanges and health technology firms rely on Surescripts to more easily and securely share health information. Ken’s responsibilities at Surescripts include monitoring and influencing state and federal laws and regulations related to health information technology, acting as Surescripts’ liaison to national and state pharmacy associations and boards, and providing guidance to the development and implementation of Surescripts programs so that they are responsive to the needs of pharmacists and the organizations in which they practice.

Prior to joining Surescripts in 2001, Ken was Vice President of Management, Professional, and State Affairs for the National Community Pharmacists Association (NCPA), where he was responsible for handling the managed care, regulatory, and operational issues that confronted NCPA’s independent pharmacy members. He also was NCPA’s liaison to all state, regional, and national pharmacy groups.  Earlier, Ken co-owned a successful independent pharmacy in western Maryland.

Ken is a graduate of the University of Maryland School of Pharmacy, is licensed to practice pharmacy in Maryland, and holds an M.B.A. from Mount Saint Mary’s University.

Brandi Van Patton

Brandi Van Patton, Pharm.D., is chief clinical officer at LogiCoy, which provides complete next generation healthcare IT solutions, including PDMP, e-Prescribing, application and data integration technologies.  Previously she was in charge of submitter compliance, data integrity, and PDMP integrations for the Nebraska Prescription Drug Monitoring Program (PDMP).

Brandi is a graduate of the Medical University of South Carolina and has practiced geriatric pharmacy for 16 years in South Carolina, North Carolina, Virginia, Maryland, and the District of Columbia.

Ann Johnson

Ann Johnson, Pharm.D., is president at Pharmacy Healthcare Solutions, LLC (PHSL) and began working for the company in 2010. PHSL provides business strategy and management consulting services to pharmaceutical manufacturers, DTx companies, managed care organizations, retail pharmacy chains, pharmacy practice management software developers, and law firms. Ann works on a variety of projects, with a current emphasis in drug compendia review and product launch support, 340B program assessment and auditing, PBM RFP support, analytics and pricing reimbursement, financial modeling, contract review, operational assessments, and policy and procedure writing and review.

Ann received her Pharm.D. from Duquesne University and graduated with a concentration in pharmacy management. She is an APPE preceptor for the Ohio Northern University Raabe College of Pharmacy and Shenandoah University Bernard J. Dunn School of Pharmacy. Ann has authored numerous articles and been published in several pharmacy journals including Specialty Pharmacy Times, Inside Patient Care, Computer Talk for the Pharmacist, and MedHealth Outlook.

Marsha Millonig

Marsha Millonig, M.B.A., B.Pharm., is the president and CEO of Catalyst Enterprises, a healthcare consulting practice helping clients achieve strategies for improved health outcomes. Marsha is also an associate fellow of the University of Minnesota College of Pharmacy’s Center for Leading Healthcare Change.

Prior to forming her company, Marsha was with the Healthcare Distribution Management Association (HDMA) and their philanthropic foundation, and the National Association of Chain Drug Stores (NACDS.) She also served as the interim executive director of the Minnesota Pharmacists Association from 2014-2019.

Marsha is a practicing pharmacist and pharmacist immunizer, working in community pharmacy. She is also a published author. Her latest work, “100 MTM Tips for Pharmacists,” is available as an e-book at the Apple Store, Amazon Kindle, Barnes and Noble, and Kobo Canada.

She received a B.S. in Pharmacy from the University of Minnesota and her M.B.A. from the University of Maryland. She completed the American Society of Health System Pharmacy (ASHP) Executive Residency in Association Management.


Tags

2024, Conferences


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