The global Cleanroom Gloves Market is estimated to be valued at US$ 1832.01 Mn in 2023 and is expected to exhibit a CAGR of 9.8% over the forecast period 2023 to 2030, as highlighted in a new report published by Coherent Market Insights.

Market Overview:

Cleanroom gloves are essential in industries requiring hygienic and sterile work environments like pharmaceuticals, medical devices, food and beverages. They protect products from contaminants and workers from hazardous materials. Major features include powder-free options, seamless construction and high sensitivity for precision work.

Market key trends:

Medical device manufacturing accounts for the largest share of demand due to rising complexity of products and stringent regulatory norms. Laminated and coated gloves providing double the barrier are gaining popularity. Growing outsourcing of manufacturing activities from developed nations and rising contract research organizations are expanding opportunities in Asia Pacific and Latin America. Strict contamination control in novel gene and cell therapies have increased adoption of gloves made from highly impermeable synthetic materials.

Segment Analysis

The global cleanroom glove market is segmented into type,form,material, and end user. Based on type, the non-powered segment dominated the market in 2022 and is expected to continue its dominance over the forecast period. This is because non-powered gloves are more economical and provide sufficient protection against contamination during cleanroom activities.

Key Takeaways

The Global Cleanroom Gloves Market Share is expected to witness high growth, exhibiting CAGR of 9.8% over the forecast period 2023 to 2030, due to increasing stringent regulatory guidelines regarding production of pharmaceuticals and medical devices. The market size for 2023 is US$ 1832.01 Mn.

Regional analysis

North America dominated the global market in 2022 and is expected to continue its dominance over the forecast period. This is due to presence of major pharmaceutical and biotech companies and stringent regulatory guidelines regarding product sterility of medical devices in countries like US and Canada.

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