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Over the past 10 years, medtech manufacturers from startups to giants have grown their levels of outsourcing to contract R&D and manufacturing partners.
September 15, 2020
By: Maria Shepherd
President and Founder, Medi-Vantage
Over the past 10 years, medtech manufacturers from startups to giants like Zimmer, Stryker, and Smith+Nephew have grown their levels of outsourcing to contract R&D and manufacturing partners. The objective of this market shift is to gain operational efficiencies, cost savings, and access to new capabilities that provide a competitive advantage. Orthopedic device companies have pivoted to concentrate on their internal core competencies. Under these conditions, outsourcing makes sense in terms of cost and speed to market if orthopedic device manufacturers select contract R&D and manufacturing partners that can expand their in-house innovation capabilities, offer scale and quality improvement, and push the fixed costs of internal R&D to the other side of the balance sheet. The drivers of this market are continued industry consolidation (driven by hospital consolidation with more expected in the future), painful cuts in reimbursement, and the driving need to rapidly innovate. Competition is increasing from every direction such as new and emerging adjacent market players like Apple and Google, digital technologies, crossover from pharmaceutical companies in the wearables space, and unknown and possibly underestimated sources of risk such as Haven Healthcare—led by Atul Gawande, M.D., MPH, and chairman of the board, which is focused on the U.S.-based employees and families from Amazon, Berkshire Hathaway, and JPMorgan Chase. Why This Is Important Contract medical device R&D has emerged as an industry of its own, with expertise at all stages of the medtech lifecycle. Sheer scale is part of the reason. FDA’s CDRH reports there are approximately 175,000 categories of medical devices available in the U.S.1 Some reports put global annual medtech sales at $425 billion in 2018 and its CAGR was forecasted (pre-COVID) to grow at approximately 5.4 percent for the near future, placing the market in 2027 at approximately $680 billion.2 Few medical device developers have the basic but broad technical expertise and resources to develop products in-house. There is a high cost to acquire that required infrastructure and expertise. Orthopedic device companies have limited finances (and all have limited budgets, especially now, in the COVID era) to maintain and manage complicated R&D programs. In addition, regulations are changing. Human factors usability testing has been mandatory since 2016 and the EU’s revised MDR will require medical devices to undergo exacting quality programs, which further escalates the need for expertise and dedicated resources. COVID-19 has delayed the enforcement of the EU’s MDR until May 2021, which will be here before we know it, so this is a “can” medical device companies cannot continue to kick down the road. Medtech manufacturers also expect outsourcing to yield cost savings and faster time to market. These are all drivers of the outsourcing of R&D, manufacturing, clinical research, and regulatory affairs. This growth will be substantial. For example, the global medtech contract manufacturing market is expected to grow to almost $100 billion by 2027 (Table 1), a CAGR of approximately 7 percent.3
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