Molecular Quality Controls Market Share, Size, Trends, Industry Analysis Report, By Product (Independent Controls, and Instrument-specific Controls); By Technology; By Application; By End-Use; By Region; Segment Forecast, 2022 - 2030
The global molecular quality controls market size is expected to reach USD 294.31 million by 2030, according to a new study by Polaris Market Research. The report “Molecular Quality Controls Market Share, Size, Trends, Industry Analysis Report, By Product (Independent Controls, and Instrument-specific Controls); By Technology; By Application; By End-Use; By Region; Segment Forecast, 2022 – 2030” gives a detailed insight into current market dynamics and provides analysis on future market growth.
Trends in the industry are driven by several variables, including the steadily rising number of clinical laboratories that are accredited. Clinical laboratory tests have aided in not just the diagnosis of disease but also in monitoring the effectiveness of treatment. Today, clinical laboratories all around the world are vying for national and international accreditation, largely to guarantee more dependable and superior laboratory services. Diagnostic laboratories conduct more intricate tests, are held to greater standards of regulatory compliance, and are subject to increased levels of regulatory scrutiny.
For instance, in April 2021, based on the results of an on-site examination, the College of American Pathologists accredited the Advanced Genomics Institute Clinical Laboratory at UC Berkeley. In the years to come, there may be an increase in demand for control solutions as a result of the urgent demand for extensive monitoring for any anomalies in diagnostic goods.
The primary factors driving this industry’s growth are the increasing use of third-party regulatory standards, the desire for external quality measurement support, the development of government funding for genomics developments, the demand for personalized medicines, the declining cost of sequencing procedures, and the increased incidence of infectious diseases, cancer, and genetic diseases.
Furthermore, in July 2021, to compete in the multiplex molecular diagnostics industry, Seegene, a significant participant, and Bio-Rad Laboratories partnered. The collaboration aims to create diagnostic solutions for infectious diseases. Additionally, subject to FDA approval and further clinical research, Seegene would provide diagnostic tests for use on Bio-CFX96 Rad’s Dx Real-Time PCR System for the American market.
As the burden of various diseases increases globally, more laboratory tests are being performed. Both public and commercial sector laboratories are opening up to address this need. To perform diagnostic tests, clinical laboratories must get accreditation from regulatory organizations such as the International Organization for Standardization (ISO) and other standards of a like kind in the majority of nations. The relevant authorities analyze a laboratory’s competency and quality system during the accreditation procedure using predetermined standards.
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