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  • Examines the impact of the US tariffs affecting the medical technology sector, announced on April 2, 2025, and implemented on April 5, 2025
  • Highlights risks to supply chain stability, cost structures, and regulatory compliance for US-based MedTech firms
  • Explains how tariff-related pressures could erode competitiveness in a globally integrated industry
  • Outlines practical strategies for adaptation, including supply chain restructuring, legal review, and operational innovation
  • Argues that MedTech leaders must move beyond crisis response toward long-term reinvention
  • Frames the tariff shock as both a disruption and a strategic inflection point for US healthcare manufacturing

The 2025 Tariff Shock

What US MedTechs Need to Know and Do

The April 2, 2025, tariff announcement by the US government - followed by its implementation on April 5 - marks more than a tactical shift in trade policy - it signals a strategic realignment of the global economic order with far-reaching consequences for the US medical technology sector. Framed as a national response to escalating geopolitical tensions and growing concerns over foreign dependency, the imposition of broad-based tariffs on imported components and finished goods aims to reindustrialise the domestic economy and reassert leverage in international commerce. Yet, for the US MedTech industry, these measures arrive not as a stabilising corrective, but as a shockwave through an already strained and highly specialised operating environment.

The global equity markets responded sharply to the news, with a pronounced - though uneven - sell-off. Certain sectors, particularly those integrated into global supply chains, bore the brunt of investor anxiety. Historically, the use of sweeping tariffs has correlated with periods of economic contraction, prompting several major economies, including the UK and EU to refrain from swift retaliatory measures in favour of a longer-term strategic posture. This suggests a broader recognition that while the US administration’s objectives may be transformative, their realisation will likely take years - during which the risk of a global recession looms large. For companies, especially those in export-reliant or import-sensitive sectors, preparedness must extend beyond trade compliance to economic resilience.

MedTech firms, unlike those in less regulated or more commoditised industries, operate within a finely calibrated global ecosystem - characterised by thin margins, rigorous quality standards, and complex regulatory oversight. Many of the now-tariffed inputs, from microelectronics to medical-grade polymers, lack viable domestic substitutes in terms of cost-efficiency, scalability, or compliance readiness. The immediate outcome is not just elevated input costs, but increased friction across procurement, manufacturing, and go-to-market timelines - posing risks to innovation pipelines, clinical delivery, and ultimately, patient outcomes.

In this new reality, US MedTech companies stand at an inflection point. The imperative extends beyond short-term cost containment or tariff navigation. It demands a broader rethinking of sourcing models, operational design, and geopolitical risk exposure. Equally, it calls for a more assertive industry voice in shaping the national trade and industrial policy agenda. For those willing to act with foresight and agility, this disruption may yet serve as a catalyst for long-overdue structural transformation and long-term competitive resilience.

 
In this Commentary

This Commentary examines the implications of the US Administration’s April 2025, tariff announcement and implementation for the American medical technology sector. While intended to strengthen domestic manufacturing, the measures risk disrupting global supply chains, increasing production costs, and complicating regulatory compliance. Against this backdrop, the piece offers strategic insights for MedTech leaders - emphasising the need for swift operational response and deeper structural adaptation to sustain competitiveness in an increasingly protectionist and volatile trade environment. The Commentary is especially relevant for healthcare professionals, directors, and executives of MedTechs, as it highlights actionable strategies to navigate the policy shift and safeguard operational and financial stability in a rapidly evolving market.
 
The New Trade Reality: What Changed on April 2

On April 2, 2025, the Office of the United States Trade Representative unveiled a sweeping tariff package aimed at reshaping global supply chains and reinforcing domestic industrial capabilities. Cast as a strategic response to intensifying geopolitical tensions and growing unease over America's dependence on foreign manufacturing, the new measures target a wide spectrum of imports from several pivotal economies - including China, Germany, and key Southeast Asian nations. These countries serve as critical nodes in the global MedTech supply chain, making the ripple effects of this policy particularly acute for US-based MedTech firms.

The newly imposed tariffs target a broad array of goods integral to MedTech innovation, manufacturing, and clinical application. Affected categories span microelectronic components critical for imaging and monitoring systems; precision instruments and surgical tools; specialty polymers used in catheters, tubing, and implants; as well as the batteries, sensors, and wireless modules that power wearable and connected care technologies. A universal baseline tariff of 10% on all imports took effect on April 5, 2025. In addition, steeper "reciprocal" tariffs - calibrated to trade imbalances and other geopolitical considerations - were levied against specific countries, with rates exceeding 25% in several cases. As of midday ET on April 8, the US imposed an additional 50% tariff on China, raising the total tariff rate to 104%. For comparison, China had previously faced a cumulative tariff of 54% - which included a 34% surcharge on top of existing duties - while Vietnam continued to face a combined tariff burden of 46%.
The economic impact of these measures is both immediate and far-reaching, with ripple effects across global supply chains and healthcare delivery systems.

What elevates the disruption is the limited substitutability of many of these inputs. Unlike sectors where domestic alternatives can be scaled or sourced quickly, MedTech depends on specialised, globally integrated supply chains. Domestic manufacturers often lack the technical capacity, regulatory readiness, or economies of scale to step in - leaving US companies little room to manoeuvre without compromising product quality, regulatory compliance, or time-to-market.

As a result, US MedTech firms are now forced to reconcile two conflicting imperatives: absorbing new cost burdens while maintaining the performance and reliability expected of their products. In an environment of heightened protectionism, this balancing act grows increasingly precarious. The tariff regime does not simply alter trade flows; it reshapes the competitive landscape, where adaptability, resilience, and strategic foresight will now define success or stagnation.

 
Immediate Business Impacts for US MedTechs

The newly imposed tariffs have unleashed a wave of immediate operational and strategic challenges for corporations. These extend beyond simple cost increases, touching every aspect of the value chain - from procurement and production to compliance and global competitiveness.

Escalating Cost Pressures and Margin Compression
Most US MedTech firms operate within rigid pricing structures, dictated by long-standing reimbursement frameworks, negotiated hospital contracts, and price-sensitive procurement processes. In many cases, there is little to no flexibility to pass increased input costs on to end buyers. Tariffs on critical upstream materials - particularly those used in high-volume, lower-margin devices - are likely to erode already thin profit margins. This is especially concerning in segments like disposable devices or basic diagnostic tools, where pricing is often commoditised and scale driven.

Supply Chain Disruption and Increased Complexity
The global supply networks that MedTech companies have spent decades optimising for efficiency are now vulnerable under the weight of new trade barriers. Tariff enforcement inconsistencies, customs delays, and increased scrutiny at ports of entry introduce volatility into previously stable sourcing arrangements. Moreover, the pressure to pivot to alternative suppliers - often on short notice - adds layers of logistical and contractual complexity, while risking bottlenecks and delayed product availability.

Regulatory and Quality Compliance Risks
In the highly regulated sector, substituting even a single component or material may trigger regulatory repercussions. The FDA often requires revalidation of manufacturing processes, quality systems, and clinical performance data, particularly for Class II and Class III devices. For implantable devices and other high-risk products, the timeline for re-approval can stretch months - or longer - posing go-to-market delays and jeopardising revenue forecasts.

Competitive Disadvantage in Global Markets
The tariffs sharply escalate costs for US MedTech manufacturers by targeting key components and materials critical to device production. With many firms reliant on global supply chains for specialised inputs, these tariffs directly inflate production costs while offering little room to offset them through price increases in a heavily regulated and cost-sensitive healthcare market.
 
Unlike competitors in Europe or Asia with diversified or exempt supply chains, US companies now face a structural disadvantage. Rising costs, combined with the complexity and delays of requalifying new suppliers, hinder their ability to compete for international tenders or respond quickly to shifting market demands.
 
Moreover, in fast-growing and highly competitive sectors - such as diagnostics, digital health, and single-use devices - even modest price differentials can lead to lost contracts or reduced adoption. As foreign buyers weigh cost, reliability, and time-to-market, US-made products risk being side-lined.
 
In effect, the new tariffs undercut US MedTech’s global competitiveness not through lack of innovation, but through increased operational friction and reduced cost efficiency. At a time when other countries are actively investing in domestic MedTech capacity, the US risks losing ground in both global market share and future leadership.

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Strategic Response: How US MedTech Companies Can Adapt

The MedTech industry has consistently demonstrated resilience in the face of adversity, whether navigating regulatory upheavals, global pandemics, or supply chain shocks. Today’s tariff-driven disruptions present another inflection point - one that forward-thinking firms can transform into a strategic opportunity. Rather than treating tariffs as just cost burdens, businesses can leverage this moment to build more agile, resilient, and innovation-driven operations.

(i) Restructure and Diversify the Supply Chain The first imperative is transparency. Corporations must conduct a comprehensive audit of their tariff exposure across their Bills of Materials (BOMs), identifying high-risk components, suppliers, and logistics bottlenecks. This visibility enables decisive action. Diversification strategies, including dual- or multi-sourcing critical inputs, can reduce reliance on high-tariff geographies such as China. Nearshoring - shifting production or assembly to proximate, lower-risk regions such as Mexico or Costa Rica - remains an option for many MedTechs aiming to reduce dependency on more volatile, distant supply chains. Under the  United States-Mexico-Canada Agreement  (USMCA), goods that meet the agreement's rules of origin continue to enjoy tariff exemptions. However, ~10% of Mexico's exports to the US, valued at ~$50bn, face challenges in meeting these compliance requirements, potentially subjecting them to a 25% tariff. Meanwhile, Costa Rica's exports to the US are now subject to a universal 10% tariff. These developments may influence the strategic decisions of MedTech enterprises considering nearshoring to these countries.​

(ii) Optimise Tariff Classifications and Legal Levers For MedTech organisations, accurate classification under the Harmonized Tariff Schedule (HTS) is critical, as misclassification can lead to unnecessarily high import duties. Given the complexity and specificity of medical devices, even minor discrepancies in classification codes can have financial implications. Collaborating with experienced trade counsel and customs brokers to audit and, where appropriate, reclassify products is often a cost-effective first step. Additionally, MedTech firms should consider tariff engineering strategies - such as modifying materials, components, or packaging - to align with lower-duty classifications without compromising product integrity or compliance. Beyond reclassification and engineering, MedTech companies should actively assess opportunities for duty exemptions or deferrals, particularly for products deemed essential to healthcare delivery or public health infrastructure. These may be available under special tariff provisions, free trade agreements, or temporary exclusions introduced through shifting trade policy in response to global health priorities.

(iii) Rebalance Financial and Pricing Models Tariffs should be treated not as isolated operational expenses but as strategic variables within broader financial planning. For MedTech CFOs, this means embedding tariff assumptions into forecasting, scenario modelling, and pricing strategies. Implementing dynamic pricing models that account for various duty situations allows for greater agility in responding to shifting trade policies or geopolitical developments. Where appropriate, consider structuring cost-sharing mechanisms with distributors, providers, or group purchasing organisations - particularly when your product demonstrably improves clinical outcomes or reduces total cost of care. This can help preserve margin while maintaining competitiveness. Additionally, evaluate the use of financial hedges or long-term procurement contracts to stabilise costs for raw materials or components subject to tariff volatility. By aligning tariff planning with financial levers, MedTech leaders can better manage risk, protect margins, and maintain commercial flexibility in an unpredictable global trade environment.

(iv) Accelerate Operational Innovation Rather than being viewed solely as cost pressures, the new tariffs present an opportunity for forward-thinking leaders to drive innovation and long-term transformation. By strategically investing in automation, additive manufacturing, and lean production techniques, companies can unlock lasting efficiency gains and build more resilient operations. Embracing digital tools - such as advanced supply chain analytics - offers improved inventory visibility and deeper insight into supplier performance. Additionally, rationalising SKUs or adopting modular platform designs can streamline logistics without compromising clinical efficacy. For leaders willing to act decisively, these changes are not just necessary - they are a competitive advantage waiting to be seized.
 

(v) Engage in Advocacy and Ecosystem Collaboration MedTech firms cannot navigate this landscape in isolation. Engaging with trade associations like AdvaMed amplifies their voice in advocating for tariff relief or more nuanced policy exemptions. Active participation in public comment processes or legal appeals can protect key product lines. Just as critical is collaboration with healthcare providers and Integrated Delivery Networks (IDNs) to ensure price transparency and maintain patient access during a time of potential cost volatility.
 
The Long View: From Disruption to Strategic Opportunity

Although the April 2025 tariffs present immediate challenges, they also open the door to a strategic inflection point for US MedTechs. Disruption - while painful - can catalyse transformation. For firms willing to act decisively, this moment offers the opportunity to rethink how and where value is created across the enterprise.

Organisations that proactively invest in supply chain resilience - diversifying supplier bases, nearshoring key components, or vertically integrating critical capabilities - will reduce long-term exposure to geopolitical and logistical shocks. Likewise, those that build regulatory agility into their operations by streamlining requalification processes and strengthening internal quality systems will be better positioned to adapt to future policy shifts without costly delays. Not to be overlooked is financial flexibility: firms that can absorb near-term margin pressures while maintaining investment in R&D and market development will emerge stronger and more competitive.

Beyond operational advantages, there is a growing reputational and commercial upside to localising production. In a climate of heightened public concern over national preparedness and healthcare security, corporations that demonstrate leadership in domestic manufacturing and supply assurance are more likely to win government contracts, forge strategic partnerships, and build trust with healthcare providers and policymakers alike.

In the long view, the current turbulence may ultimately favour those firms that view trade disruption not simply as a constraint, but as a catalyst for reinvention - a chance to align operational strategy with national priorities and global resilience.

 
Takeaways

For US MedTech leaders, the current-2025 situation demands swift, coordinated, and strategic action. The new tariff landscape is not just a policy shift - it is a stress test for organisational resilience and a proving ground for leadership. To navigate this environment effectively, enterprises must break down internal silos and align cross-functional teams - spanning legal, operations, finance, and regulatory - around a unified response strategy. A coherent plan is essential not only for mitigating near-term disruptions but for preserving long-term competitiveness and credibility in the eyes of all stakeholders.

Transparent communication is equally important. Customers, investors, and supply chain partners must understand how your business is responding and what it means for continuity, quality, and cost. Openness fosters trust - and in times of uncertainty, trust becomes a strategic asset.

Most significantly, this is a moment to look beyond survival. Use this disruption as a catalyst to stress-test your systems, identify vulnerabilities, and turn risk into opportunity. Build the agility now that will define the winners of tomorrow.

Healthcare does not pause for policy changes - and patients cannot wait. The same urgency that drives innovation at the bedside must now be applied to strategy in the boardroom. The time to act - clearly, decisively, and collaboratively - is now.
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  • Traditional spine companies’ supply chains are linear, labour intensive and siloed and their inventory-to-revenue ratios tend to be high
  • To remain relevant in an environment where the physical and digital worlds are converging company leaders will need to improve their supply chains
  • Digitalization can help achieve this but requires embracing data management techniques
  • As a response to the COVID-19 crisis some MedTech’s introduced and extended their digital strategies
  • Have they done enough to remain relevant in a rapidly evolving ecosystem?
  
- Low back pain and the global spine industry -
 
Digitalization: the reinvention of spine companies’ supply chains and controlling the inventory-to-revenue ratio
 
In 2020, spine companies, like most MedTechs, absorbed shocks of the COVID-19 crisis by digitizing aspects of their supply chains, which consists of a wide range of transactions and constitute a significant part of a company’s’ total value creation. Industry observers are asking: Will enterprises extend their digitalization strategies and emerge stronger after the impact of the pandemic, or will they reduce their digital activities and emerge weaker?

 
Market changes

Even before the COVID-19 pandemic, the days of business-as-usual for spine companies were numbered as technologies advanced, regulations became more stringent, populations aged, healthcare systems struggled with unsustainable costs of surgeries for common age-related degenerative disc disorders, and payors tightened their reimbursement policies. In the US, which is the biggest market for spinal implants and devices, an increasing percentage of people have become covered by Medicare and Medicaid [state and federal government healthcare programmes], which reimburse providers at a fraction of private healthcare insurance levels. These changes encouraged independent hospitals in the US to join purchasing syndicates, clinicians to give up private practice and become salaried employees of hospitals, and private payors to shift away from a fee-for-service provision towards a value-based reimbursement approach focussed on improving patient outcomes and lowering costs. This shift encouraged policies to keep patients out of hospitals and increased the utilization of outpatient settings and other measures expected to improve outcomes and generate shared savings.

The structural headwinds described here have not abated and are likely to intensify over the next five years. To prosper in this evolving ecosystem, companies will need to devise and enhance solutions that bring enhanced clinical benefits to patients and economic rewards to the system. Tried and tested and widely used digital strategies can help to improve supply chains. However, while these structural changes have been progressing, spine market supply chains have tended to remain linear and labour-intensive and are now becoming significant obstacles to change, while producing infrastructures with unsustainable costs.

 
In the Commentary

This Commentary suggests that, over the next five years, market forces will oblige spine companies to pivot away from their inefficient supply chains and start developing supply networks, predicated upon digital strategies that add value to patients and reduce costs. Such systems, employ common digital applications that are used extensively in other industries to ensure the right products and services are delivered to the right place, at the right time, at the lowest cost. This would constitute a “first step” in a bigger digital transformation of the spine market, which will be necessary to create new levels of productivity, growth, and sustainability. We suggest that the reluctance of some MedTech’s to transition from inefficient supply chains to efficient ones could be explained by a significant proportion of their C suite members not acquiring a familiarity with digital systems until much later in their careers when they were adults. The Commentary uses two concepts: ‘digitization’ and ‘digitalization’. The former is a process to convert various physical signals into digital formats and the latter leverages digitized information to improve business processes.
 
Digitizing supply chains

Over the past two decades the cost of digital technologies has plummeted while their power and capabilities have substantially increased. This has enabled business leaders to combine technologies associated with information and operations and empowered them to create value in new and different ways. Improved processing capabilities now augment human thinking to analyse more data more quickly, and then act upon the outcomes. Such changes have ushered in the new digital era for MedTech’s.
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However, the spine market has been slow, compared to other industries, to adopt digital supply networks. The process of developing such strategies to drive productivity, while absorbing the shock of a pandemic has not been easy as it meant installing new technologies under pressure. However, the COVID-19 crisis created an incentive to reconfigure operations. The companies that did this have an opportunity to develop an omnichannel [multichannel approach to sales and marketing] dedicated to enhancing engagements with healthcare professionals and improving the overall quality of care, patient outcomes, revenues, productivity, employee satisfaction, and talent attraction and retention. But this will mean companies establishing virtual options as a core competence and reinventing the way they engage with stakeholders to provide a seamless experience across digital, remote, and in-person channels.
 
Neo Medical and value-based spine care
 
A firm that has employed digital strategies to streamline part of its supply chain to enhance value and gain a competitive edge is Neo Medical, a privately held Swiss company founded in 2013 by two former Stryker employees. The company has developed a universal value-based surgical spine platform to provide patients with high quality outcomes at relatively low costs. Neo’s approach is predicated upon its ability to reduce an instrument set, comprised of >200 screw sizes to 14, and use it in a novel approach to thoracolumbar fusion. [The thoracolumbar spine is the area between your stiff thoracic cage and your mobile lumbar spine].

Neo refers to its solution as a ‘controlled fixation’, which is beginning to have an impact in markets across the EU-27, Asia-Pacific (APAC) and more recently, the US. The approach is designed to facilitate an anatomically neutral, balanced, and stable spine load bearing to achieve a more functional fusion. It is reported that the platform: (i) enables clinicians to limit stress overload on a patient’s spine and thereby reduces the risk of screws loosening and hardware failing, (ii) limits infections, (iii) removes the need for re-sterilization, (iv) declutters the operating room, (v) reduces revision rates and (vi) cuts costs.Equally important are Neo’s digital strategies to provide an easier and more efficient experience for patients, surgeons, and hospitals.

Findings of a study, published in the December 2020 edition of Interdisciplinary Neurosurgery,  suggest that Neo Medical’s value proposition saves costs by: (i) reducing supply chain processing and logistical expenses, (ii) decreasing rates of contaminated instruments, (iii) minimizing operating room delays and (iv) potentially lowering revision and infection rates.

 
Reconfiguring the supply chain

By contrast, traditional industry supply chains tend to be linear, labour intensive and siloed. As suggested by Neo Medical and others, digitalization can transform these inefficient systems into dynamic, interconnected efficient networks with the capacity to accommodate a range of stakeholders simultaneously. The shift from linear, sequential structures to interconnected, open supply operations could provide a foundation for how spine companies compete in the future.
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Companies in other sectors have already made such transformations and integrated their supply networks into their operations and decision-making processes with the objective of gaining competitive advantages. However, business leaders should be mindful that the more customer focussed enterprises become, the more developed their data and analytical capabilities must be.
Currently, few MedTech’s integrate their supply chains into their long-term strategies, and few actively and fully embrace the potential of data management techniques. This reluctance decreases a company’s ability to optimize inventories and enhance operational efficiencies of product offerings moving across supply chains. Given the increasing number of exogenous forces affecting the spine market, [e.g., ageing populations, vast and escalating healthcare costs, more stringent reimbursement policies, pricing pressures, tightening regulations, increasing competition, advancing technologies and heightened customer expectations], it seems reasonable to suggest that investing in and developing digital supply networks could be a logical step to enhance value agendas.

Appropriate digitalization of supply chain planning and processing could help to: (i) reduce operational siloes, (ii) respond effectively to market disruptions, (iii) minimize the time, costs and risks associated with onboarding and collaborating with suppliers, (iv) deliver products and services that customers need, when they need them, where they need them at the lowest cost and (v) enable end-to-end supply chain visibility and transparency to facilitate gathering and analysing real-time intelligence to enhance efficiencies.
 
C suites and digital immigrants
 
Given that there are significant advantages in adopting digital technologies, why is the spine market lagging other industries in adopting such strategies to improve its supply chains to enhance its productivity and sustainability? A preponderance of digital immigrants among C suites could help to explain why some MedTech’s fail to grasp the full potential of digitalization strategies. Let us explain.
 
According to research undertaken by Korn Ferry, a consulting firm, the average age of a C suite executive of the top 1,000 US organizations is ~57. Statista confirms this and reports that in 2018, the average age of CEOs in US at the time they were hired stood at 54 years, while the average age of CFOs when they were hired was 50. Since 2005 the average age for CEOs and CFOs has been trending upwards. To the extent that these data are indicative of MedTech’s, it seems reasonable to suggest that their C suite members: (i) would have completed their formative schooling before the digital era, and (ii) when they started their professional careers the digital age was just beginning. For example, in 1989 only 15% of US households owned a personal computer, <1% of the world's technologically stored information was in a digital format, and the World Wide Web did not become publicly available until 1991. In 1990, when the average C suite member would have been ~31, there were only ~12.5m cell phone subscribers worldwide; ~0.25% of the world’s population, and Internet users only amounted to ~2.5m; 0.05% of the world’s population. In 2002, when the average US C suite executive would have: (i) been ~37, (ii) completed their professional training and (iii) well into their careers, digital technologies were still relatively underdeveloped. For example, cell phone subscribers were only ~1.5bn; 19% of the world’s population, and Internet users were only ~631m; 11% of the world’s population.
 
This suggests that during C suite executive’s formative education and professional training, digital technologies were embryonic, and the Internet, mobile devices, social networking, big data, and computing clouds, had not yet transformed work practices and healthcare. Thus, a significant proportion of current executives of US MedTech’s could be digital Immigrants: people whose professional careers were influenced by analogue technologies, paper, and television, and they only acquired a familiarity with digital systems later in their careers when they were adults. This could affect their ability to appreciate the full potential of digital technologies and help to explain the relative reluctance of MedTech’s to digitize labour intensive, inefficient, linear supply chains.
Stringent regulation and digitization
 
This reluctance becomes more significant as regulators demand that MedTech’s employ more sophisticated digital strategies. Increasingly, people are being given spinal implants and devices, which cannot be subsequently removed. Patients rely on these to be safe and to perform as intended for their lifetime, and regulators are devising more stringent rules to ensure that this is the case. For example, the European Medical Device Regulation (MDR), which entered into force in May 2017, requires all medical devices sold in the EU-27 and Switzerland to be MDR approved. The EU-27 represents ~33% of the spine market’s global revenues. MDR governs the production and distribution of medical devices and their compliance. The regulation states that, “Medical device manufacturers are required to have systematic methods for examining their devices once available on the market, by systematically gathering, recording, and analysing data on safety and performance”. MDR expects all MedTech’s to have robust supply chains and the ability to conduct data-driven audits to trace manufacturing modifications to specific implants and devices and to prove the resolution of any problem that might arise. While tightening regulations increase approval costs and prolongs product development time, they also provide incentives for companies to enhance their digital supply networks.
 
Controlling the inventory-to-revenue ratio
 
A digital supply network can enhance an organization’s ability to manufacture products in optimum volumes and deliver them to the right customers at the right time. This could help to improve patient outcomes and lower costs. Also, digitalization assists enterprises to enhance the control of their inventory by improving planning, forecasting and management, which is critical given their relatively high inventory-to-revenue ratios.

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Spine surgeons in hospitals need to have relevant implants and devices available in the operating room at the right time. Hospitals need to be able to locate products in their cabinets. Without appropriate digitalization strategies health professionals would need to spend time searching for devices that may or may not be used during an operation. This means increased costs, as high value surgical trays would flow through inefficient supply chains.

To reduce costs, hospitals and healthcare systems push the responsibility for inventory management onto their suppliers. This results in a range of different models, which tends to increase the risks to manufacturers. Currently, spine companies manage a range of different types of inventories, with a significant proportion of their product offerings being held either on consignment or by sales reps, who often spend time managing offerings on behalf of their customers. This increases the difficulty to accurately account for supply levels, location, ownership, and usage, which further complicates billing and replenishment and often leads to excess inventory and unnecessary costs.  
A digital supply network can help to reduce these inefficiencies by eliminating waste and saving costs for all stakeholders. Typically, spine surgical sets contain several types of devices, plates, and screws, and usually are sold on consignment. Hospitals return these for re-provisioning often after only having used some of the items in the trays. To guarantee that sales-reps and hospitals have sufficient supplies, manufacturers maintain relatively large, consigned inventories, at significant costs, which impact on the rate of excess and obsolete inventories.
 
A digital supply network effectively connects manufactures with their sales-reps and hospitals to reduce inefficiencies. Surgical trays are tagged with radio-frequency identification (RFID), so they can be effortlessly tracked by hospitals’ smart cabinets and by all other stakeholders. This allows: (i) hospitals to be billed as soon as a surgical tray, or a part of it, is removed, and the replenishment process started, and (ii) suppliers to reduce their consigned inventory, reduce their excess and obsolete inventory, and reduce their costs.
 
Ethical issues

We have broached some of the functional benefits and challenges of digitizing supply chains. Before closing, let us briefly draw attention to some ethical issues associated with digitization, which include increasing the challenges associated with data privacy, cybercrime, and the need to keep pace with new and rapidly developing technologies. This gives weight to environmental, social and governance (ESG) agendas, which are positioned to play an increasingly prominent role over the next five years and shall be discussed in a future Commentary.
 
Takeaways

We have made some suggestions about how common digitalization strategies could improve spine market supply chains and create added value for patients while delivering the highest sustainable returns for manufactures. We have also suggested reasons for the reluctance of some companies to employ digital strategies to transition from linear labour-intensive supply chains to supply networks. In response to the COVID-19 crisis, many organizations partially digitized their supply chains to sustain trading during what became a “new normal” of remote engagements. This suggested that digital enhancements could help spine companies improve their way of working, expand access to services, and deliver more valuable patient-clinician experiences. Dynamics within sectors usually change after a crisis. For example, following the 2008 economic crash, strong companies emerged stronger while weak companies emerged weaker.  A defining difference between the strong and the weak was resilience: the ability not only to absorb shocks, but to use them to transform supply chains and enhance competitive advantage. Will spine companies emerge from the COVID-19 crisis stronger and extend their digitized supply networks or will they revert to their costly and inefficient labour-intensive linear supply chains? Keep an eye on the inventory-to-revenue ratio.
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