UK: +44 (0)1223 264428
USA: +1 (919) 901 0909
by Ben Strutt
The consumer health sector is expanding fast. From its traditional base, the category has exploded to deliver a myriad of products for consumers to manage everything from personal health and hygiene to fitness and pampering treatments.
This explosion has several directions. Established healthcare companies which have an appetite to build more ‘sticky’ customer relationships and new revenue streams are adopting techniques from the fast-moving consumer goods sectors – such as psychology, brands and sensory dynamics – to build revenues. Meanwhile, consumer goods companies are keen to exploit their established brand equities and credibility to deliver new wellbeing products. Digital technology is also opening the door to disruptive opportunities for tailored personal health experiences – such as systems that identify almost imperceptible, long-term changes that underpin self-diagnosis and treatment. A plethora of start-ups is taking full advantage in fields such as fertility, sleep and stress management. At the other end of the scale, Amazon’s increasingly clear interest in strategic healthcare partnerships is making some of the established industry leaders nervous.
The underlying drivers of this growth include an affluent ageing population, the so-called ‘grey pound’; shrinking public healthcare budgets limiting access to conventional healthcare; conventional healthcare moving from the clinic to the home to save cost; and increasing consumer awareness of what’s good and bad for our health, driven by the media and the power of the internet. These factors are growing an appetite for new tools that enable self-diagnosis and therapy.
A feature of this market is the complex international regulatory landscape, and the significant additional costs and timescales associated with bringing regulated medical devices, diagnostics and pharmaceuticals to market. For example, therapeutic options may be fully licensed pharmaceuticals, over-the-counter medicines, unlicensed under ‘grandfather’ rules or just foods – resulting in consumer confusion and questions over safety, efficacy and therapeutic claims.
For example, the flood of Chinese e-cigarettes emerging onto the market in the last 10 years gave consumers a heralded ‘reduced-risk’ alternative to tobacco but with little in the way of quality standards or evidence to support that assertion. The European Union Tobacco Products Directive took some time to catch up and establish a base line for product safety – and, in the US, the regulatory landscape is still in flux.
Public perception is changing, too, about how and where products should be used. Carbamide peroxide – less glamorously known as urea peroxide – was developed and patented in 1989 as a professional tooth whitening treatment. It transitioned 0ver the following 20 years into a range of products sold for use at home. Public fears, it would seem, have been allayed by the easy access to these products that are often promoted by small companies with little to lose, using low-cost marketing strategies – and the products are not without potential dangers when you consider the high concentrations of peroxide being applied to the mouth.
Another example is the ‘sexual wellbeing’ category that has become mainstream as ‘sex toys’ arrive on our supermarket shelves. Devoid of regulation, only three therapeutic vibrators meet Food and Drug Administration requirements for specific medical applications, although some of the most responsible manufacturers are taking voluntary steps to ensure product safety to protect their customers and brands – for example, by using phthalate-free, medical-grade polymers and offering product cleansing solutions. But as the recent $3.75m connected We-Vibe data protection breach shows, the risks to users from such devices can be digital as well as physical – highlighting why consumer healthcare businesses need high standards that may be outside their governance capabilities.
Another factor to consider is that the new European Medical Devices Regulation suggests that ‘consumer health’ may not even exist as a sector in the future – as all devices will be considered medical devices if they look like a medical device.
A technical ability to deliver a new product to market is only one element of a landscape of commercial challenges facing the emerging wellbeing category. People increasingly want to manage their own wellness and they deserve to be able to choose from honestly marketed, safe, effective and increasingly tailored products and services. The brands that win will do so through exemplary science, design quality and standout user experiences that deliver against real unmet needs, underpinned by a responsible approach to commercialisation.
The ISO 11608 series of standards are undergoing fundamental change - what should parenteral device companies be expecting?
01 April 2021
Unique perspectives as four of our leaders reflect on how their gender affects their work in innovation and design.
16 December 2020
Stay up to date with all our work and our latest news by signing up to our newsletter.