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The FDA approvals of Roche Holdings’ (OTC:RHHBY) Hemlibra or Cobas Cdiff Nucleic acid test and Thermo Fisher Scientific’s (NYSE:TMO) slew of advancements in next-generation sequencing (the latest one being the FDA approved Oncomine Dx Target Test) clearly point toward the rapid emergence of in vitro diagnostics (IVD) in the MedTech space.
The recent EvaluateMedTech World Preview indicates that while worldwide MedTech sales are expected to witness CAGR of 5.1% to $522 billion by 2022, steering ahead of cardiology, IVD will rake in annual sales of $69.6 billion at a CAGR of 5.9%.
The above data is just a small indicator of the vast scope for growth of the IVD market. For investors keen on MedTech, the most important fact is that IVD’s benefits are not limited to any particular country or geographic territory. With the emergence of complex and transmittable diseases worldwide, this part of the MedTech space is currently in the spotlight.
IVD in a Nutshell
If we go by FDA’s definition, in vitro diagnostics are, “tests that can detect diseases, conditions, or infections. Some tests are used in laboratory or other health professional settings and other tests are for consumers to use at home.”
Growth Factors
Rapid occurrence of infectious diseases worldwide, increasing burden of killer bugs like cancer, cardiovascular diseases, stroke and other heart diseases, and diabetes in developing and developed nations as well as growing cognizance of early cancer screening, detection, and prevention have made IVD indispensable in the healthcare space.
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