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Close-up of a cleanroom technician's gloved hand placing a delicate sample into a circular analytical instrument inside a sterile, ISO-classified laboratory environment.

Cleanroom Gloves & Vendor Selection: Recommended Practices

Cleanroom gloves play a vital role in contamination control. In this chapter, discover how to evaluate glove options to balance protection, comfort, and performance effectively. You will learn:
  • The critical role gloves play in contamination control
  • Key performance criteria for cleanroom gloves
  • Challenges in balancing glove cleanliness with operator comfort
  • How to interpret testing methods and certification data

 

This article is Chapter 2 of Valutek's Technical Paper Series:
Cleanroom Gloves & Vendor Selection: Recommended Practices

The Importance of Cleanroom Gloves

Gloves are the most frequently used cleanroom consumable and act as the direct barrier between operators and critical products. Their primary function is to protect products and processes from contamination while ensuring operator safety and comfort during extended wear periods.

Selecting the right gloves requires balancing protection and comfort. Gloves must fit well, provide sufficient dexterity, and comply with contamination control standards to minimize particle shedding and chemical residue.

Performance Criteria for Glove Selection

Glove materials typically include nitrile, latex, and PVC, each offering distinct advantages:

  • Nitrile: Preferred for chemical resistance and durability without latex allergens.

  • Latex: Offers excellent tactile sensitivity but may cause allergies.

  • PVC: Cost-effective and chemically resistant, though less flexible.

Critical selection factors include:

  • Cleanliness and Packaging: Gloves should be vacuum-sealed in double bags with cuffs oriented for easy donning and reduced contamination risk.

  • Cuff Length: Gloves must overlap the cleanroom garment sleeves to prevent exposed skin contamination.

  • Durability: Tensile strength and thickness affect glove longevity and protection level.

  • Comfort & Fit: Proper fit reduces hand fatigue and improves dexterity.

  • Electrostatic Discharge (ESD) Properties: Essential in environments sensitive to static.

Balancing Comfort with Contamination Control

Gloves with the highest containment efficiency are often thicker and less flexible, potentially decreasing operator comfort and productivity. It’s crucial to involve operators in the selection process to identify gloves that meet cleanliness requirements without sacrificing comfort. Launderable glove liners can be used to enhance comfort and extend glove wear time.

Testing and Certification Standards

Reliable glove selection depends on rigorous testing and certification. Vendors should provide test results for physical properties (e.g., tensile strength, elongation), contamination levels (e.g., particle counts, chemical residues), and electrostatic properties according to ASTM and IEST standards.

Emerging technologies like Scanning Electron Microscopy with Energy Dispersive X-Ray Analysis (SEM-EDX) enable detection of microscopic contaminants on glove surfaces, enhancing quality assurance.

“Selecting a glove that is both clean—to prevent product cross-contamination—and comfortable—to drive operator efficiency—is mission critical.”
— Jan Eudy, Cleanroom and Contamination Control Consultant

Key Considerations for Implementation

  • Develop internal specifications based on cleanroom classification and process needs.
  • Collaborate with vendors to obtain third-party validated test data.
  • Engage operators in trials to assess comfort and fit.
  • Establish protocols for glove storage, handling, and donning to maintain cleanliness.
Choosing the right cleanroom gloves enhances contamination control and operator performance. Armed with this knowledge, your cleanroom can maintain strict standards while supporting efficient operations.

 

EXPLORE MORE RESOURCES

Jan Eudy is a cleanroom/contamination control and microbiological subject matter expert with more than 30 years of industry experience in semiconductor, microelectronics, pharmaceutical, biopharmaceutical, medical device, food manufacturing, compounding pharmacies, aerospace, and automotive. As the corporate quality assurance manager for Cintas Corp., Jan oversaw research and development, directed the quality system and ISO registration at all cleanroom locations, and supported validation and sterile services. During her time with the company, Jan also implemented and maintained the HACCP risk management program at all Cintas industrial laundries. She is also a Past President and Fellow of the Institute for Environmental Sciences and Technology (IEST).