Yes true. The COVID vaccines, were the first time a lot of people got an insight into clinical trials and the approval process for a medicine. Large numbers of people were discussing all of that online, which you wouldn't typically see in a clinical trial.
We've seen a lot of "perception is fact" in during the COVID pandemic. We had a lot of people on Facebook talking about how it was 5G or the government implanting a chip or something, which is factually incorrect. But also, there's been a lot more awareness of the fact that yes, there were long regulatory processes in trials that needed to be gone through, but when push came to shove, actually those processes could be shortcut and could be shortened significantly. And a viable treatment was produced at the end. In fact, several were, and the same for diagnostics. So at some point, people will start to go, well, so if we could do this here, why over here are we still taking this long? Why is COVID more important than, for example, cervical screening, breast cancer or prostate cancer? Why is that we able to do it here, but not here?
It's an interesting point you raised in terms of customer and public expectations. We’ve seen people now expect the same level of communication personlisation from healthcare companies, as they would from a consumer facing business like Amazon. They want us to meet them at a time and place that suits them with highly relevant content. Pharma can't afford to ignore that customer expectation.
No, exactly. That brings us to another thing we need to consider - our regulations when it comes to what we are and are not allowed to say direct to the public. It’s all well and good, but it presupposes this world where if we decide not to say it, that information does not exist on the internet. But people go onto Google- with its 1.2 trillion searches - a year and find it anyway, because it's available elsewhere. So I think we also need to be mindful when we approach regulatory affairs and when we approach regulation in Australia, that yes we're an island, but we're really not when it comes to information. We are a small part of a massive world, and the information is already available.
And if that information is not there from a reputable source, such as the treatment provider, it's probably going be people’s anecdotal experiences and word of mouth that fill the void.
Exactly. And you think about the rise of influencers on social media over the last few years. There's no requirement for influencers to have any particular background or qualifications. They can say pretty much what they want to say as long as it's not libelous. And people will listen and believe it because they're the influencer, it doesn't have to be factual.
The TikTok Ozempic conversation was an interesting play out of that scenario where not only did you have a huge volume of people talking about this treatment without any clinician input in that conversation, but then it also led to a whole lot of people requesting off-label weight loss prescriptions. The nuance that the treatment was approved for type 2 diabetes didn’t really make its way into a TikTok conversation for some time.
No, it absolutely didn’t. Probably the most famous example of an influencer who is able to say something that is completely off the charts incorrect when it comes to healthcare and therapeutic goods, would be Donald Trump suggesting people inject bleach to help with COVID. That is a classic example, because there were probably people who believed that. That's quite scary, but it also points to the fact that social media and the availability of all sorts of unmoderated information globally means that some of our regulatory processes may need to be reviewed in that light. It just comes back to not kidding ourselves, we can't close the walls and say, if it's not an Australian TGA approved website or Medicine Australia approved website, no one can ever find it. That's not the reality we live in.
In the current constraints of our regulatory guidelines, how can teams balance the desire to provide the most useful, current, relevant information and the need to keep campaigns compliant? What specific strategies or tactics can pharma marketers use to balance innovation and compliance?
It's a real challenge. I can speak primarily from the diagnostic side as I've not been involved on the pharma side, but I think in a similar way to needing to take the individual's bias out of how we achieve the strategy - I think that organisations in healthcare might need to take themselves out of some of their go to market.
For example, let’s look at prostate cancer, and the early diagnosis and then treatment for prostate cancer. Imagine a world where the only effort that every single commercial entity in Australia, that had any relevant product or service in this space, did was devote themselves to educating the public on the importance of early diagnostics and screening for prostate cancer and then on the effective treatment for prostate cancer. We’d have a well-informed, educated population who can go and have well-informed, educated and aware (and early) conversations with their clinicians, and then have better health outcomes because they actually understand the impact of the regular screening and the treatment. In that world, it wouldn't matter whether you talk about your product or service or not.
So, if you take yourself out of it and you just talk to the patients about the things they need to know, which is why diagnostics is important, and how much of a difference it can make to their life, that's probably the most effective thing that we as a healthcare industry could do to change the game in terms of how we communicate.