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Showing 1-14 of 14 results for "gloves" within Site Content
Detection of Low Bacterial Contamination from Neoprene® Gloves with ICR Swabs
The ICR swabs and ICR contact plates are designed for environmental monitoring i.e., detection and enumeration of microbial contamination on dry, flat, and hard-to-access surfaces in cleanrooms and isolators.
Histopaque® Density Gradient Media Troubleshooting Guide
This troubleshooting guide addresses the most common sources of error observed when using Histopaque but is not meant to be a comprehensive list.
RNA Preparation Troubleshooting
This page shows possible causes and solutions for problems that may occur during RNA preparation.
Chemical and Microbiological Monitoring for Breweries
Learn more about chemical and microbiological monitoring in breweries.
Getting Started in 3D Cell Culture and 3D Bioprinting
Getting Started in 3D Cell Culture and 3D Bioprinting
Evaluating USP 665 for Extractables Testing and Reducing Animal Testing for Biological Reactivity
In this webinar, you will learn about the new and changing compendial methods and what it means for pharmaceutical manufacturing.
Surface & Personnel Testing
Surface monitoring and personnel monitoring measure the levels of microbial contamination in production areas to control the measures of disinfection routines.
Quantum Dots: An Emerging Class of Soluble Optical Nanomaterials
We presents an article concering Quantum Dots: An Emerging Class of Soluble Optical Nanomaterials.
Bacterial Retention Testing
Required by regulatory bodies worldwide, bacterial retention testing (BRT) is a critical step in filter validation. Our skilled validation specialists conduct BRT using each end-user’s worst-case biopharmaceutical processing conditions to ensure a best-case outcome.
Filter Integrity Testing
Our integrity testing for sterilizing-grade filters can help you set a test specification for your drug product, then check for leaks or filter damage using pre-use and post-use testing as recommended or required by regulatory agencies and the Parenteral Drug
Extractables and Leachables
Proving that extractables and leachables from your process aren’t harmful to the final drug product is easier with BioReliance® Validation Services. Our extractables and leachables (E&L) services thoroughly evaluate all contact materials and processes to mitigate concerns about process fluids.
Validation Service Levels
Discover an easier way to global compliance with our validation services, simplifying your process from the start with two predefined service levels and globally harmonized testing.
Chemical Compatibility Testing
Our physical and chemical compatibility testing services help you comply with GMP guidelines worldwide, proving that your biopharmaceutical filters and single-use systems are not reactive, additive, or absorptive upon contact with drug product.