Interview
Data-first: AI governance a fundamental pillar in the hospital pharmacy
AI is having a pronounced impact in the hospital pharmacy, with data quality considerations remaining a topmost concern. By Ross Law.
Main image: Michael Palone, global pharmacy leader at Swisslog Healthcare.
Main video credit: ptgregus/Shutterstock.com
The explosion of artificial intelligence (AI) since OpenAI's ChatGPT became publicly available in late 2022 has led to the technology’s deployment across multiple fields, not least in the pharmaceutical industry.
Within the hospital pharmacy, AI is taking on roles such as routine dispensary automation and inventory management while also assisting clinical teams with real-time patient data analysis, and even forecasting drug shortages. By streamlining such administrative and logistical processes, the technology allows pharmacists to dedicate more time to high-value clinical activities and direct patient care efforts.
This innovation drive for healthcare providers (HCPs), however, requires due diligence, with AI proponents highlighting that it remains important for pharmacists to understand the technology’s most effective uses, limitations, and best practice governance.
With its potential to hallucinate and make errors, caution should be exercised in AI’s applications. The American Society of Health-System Pharmacists (ASHP) advocate that pharmacists must lead the design, validation, and governance to ensure AI tools augment rather than replace professional clinical judgment.
With increasing deployment of AI in the pharmacy, governance strategies for HCPs are of rising importance. Pharmaceutical Technology spoke with Michael Palone, pharmacy affairs executive at healthcare logistics and automation company Swisslog, to learn more about AI governance in the hospital pharmacy context, what challenges exist, and what the best practices for the technology’s implementation into pharmacy workflow protocols should be.
This interview has been edited for length and clarity.
Global pharma supply chains are susceptible to disruption due to geopolitical, natural disasters, and pandemics. Credit: IM Imagery/Shutterstock.com
Even “Acts of God” reveal limitations in supply chain agility. A case in point was the severe shortage of IV fluids in the US after damage to Baxter’s North Carolina-based facility during Hurricane Helene in September 2024.
With market dynamics in constant flux, Pharmaceutical Technology spoke with Stefan Verheyden, CEO of Sanner, a German-based CDMO for pharmaceutical and medical device packaging, to discuss how the healthcare industry is built to withstand disruption.
The interview was conducted ahead of Pharmapack Europe, a pharma packaging conference held from 21 to 22 January in Paris.
This interview has been edited for length and clarity.
Ross Law: What are the key considerations regarding AI governance in the pharmacy space?
Michael Palone: Regarding data and AI, we can draw a lot from clinical information more broadly. Over time in healthcare, we’ve built a good understanding of how to assess clinical tools; we rely on expert content, so in the pharmacy instance, we may have 10 or 15 of our most-vetted, best evidence-based tools that we use – whether it's dose adjustments or applicability for antibiotics to guide medication management.
I think the same principles apply to AI, which is what's the data source? We learned a lot during Covid that all medical information is not good medical information, and now, with it all at our fingertips, it's all the more important that we point these AI tools at vetted information, and the higher quality information that we have, the better our outcomes will be.
As it relates to data integrity, we need to have transparency with our partners, and to challenge vendors on what their pool of data is, and what are we feeding the AI to help give us good information and ensure it performs accurately.
Clinical information is not universal; we know that there's genomic differences for medications and that what works for one individual may not work for someone else within different culture, ethnicity or sex, so the sufficiency of the pool of data becomes a key question. And then, naturally, the backbone of everything today is security, and understanding whether data is being used well and ethically, and if it's being combined with other data, ensuring it's not identifying individuals on a personal level.
Ross Law: What are your key concerns around AI’s deployment in the pharmacy space?
Michael Palone: As a caregiver and a patient, we want the data to be as vetted and as accurate as possible, and sometimes I worry about the speed of adoption and making sure that we're not putting the engine ahead of the dataset. There’s all this great work being done on the speed and the power of our engines, but I don't hear as much as I'd like to about the data source. And if we put those two things together, a really great data source with good quality and security, combined with all the incredible things being done with engines, then we have something massively powerful. But if either of those two things aren't working well together, then we have a mess.
Ross Law: Does this suggest human-in-the-loop remains a key aspect of AI’s deployment in the hospital pharmacy?
Michael Palone: I think so. My colleagues would make the argument that we benefit from good reference data, and AI bringing that to us and not making us search. You might go through two or three different resources to get an answer to a clinical problem. It's wonderful if AI can help us sum up that good information, and then we can make the final determination on whether or not it's applied. So, we speed up the process by using AI, but as clinicians, we are ultimately responsible for making the decision, and we can’t deflect that onus to an AI tool.
Ross Law: In rationalising the approach to AI governance, where should the responsibility sit?
Michael Palone: If we lean into what we've learned about clinical research studies, most organisations globally that are involved in these sorts of studies, whether drug studies or others, have well established protocols such as having good documentation and regular reviews.
I think we can adopt what we've learned about clinical research over the last 20-30 years to AI. It's not exactly the same, but if you think about some of the concerns, risks, and sensitivities around clinical research, they can readily be transposed to an approach towards AI’s implementation. I think you need to have the people on the ground, whomever is using the tool from the real world experience side, along with IT security teams and, CIOs, and vendor partners. That's how we'll make these tools really valuable.
Ross Law: Regarding AI, how does predictive inventory management intersect with regulatory compliance and drug shortage management?
Michael Palone: When we hear from our customers, the one thing that strikes me is that if I ask a pharmacy director anywhere in the world what their number one challenges are, it's drug shortages and staff.
Everybody's struggling with the same thing, and drug shortages require an awful lot of time to manage, so this is an example where AI and good algorithms can go a long way to being a good tool for the buyers in pharmacies.
There’s little regulatory guidance on these things, but organisations are getting better about reacting. Being more proactive means that they may be able to pivot and ensure that they have some parallel clinical treatments for something that's not available. But if you can't get a bag of normal saline, that's hard to replace, and AI won't solve that problem for you.
We typically manage our inventory in a very old school manner in hospitals. We have expected stock levels and we replenish to that stock level, but care is much more dynamic than that today, and that's where AI can really make a difference.
Ross Law: Do you foresee more guidance coming from industry around best practice regarding AI governance in the pharmacy?
Michael Palone: In areas like clinical research, there is less actual regulation, and more of a focus on best practices the industry adopts. I expect that AI will probably follow a similar course, especially since it’s difficult to get lawmakers to understand this area given it’s not their strength. Organisations within the pharmacy industry such as the Society for Hospital Pharmacy have already offered up guidance surrounding key considerations for AI governance, and over time, I think it will evolve into good standards of practice if we’re doing it right. If we have harm, then that is when lawmakers often respond and move towards legislation, but if we're doing it right, we can use our professional organisations in a positive way to handle such governance functions.
