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Pharmaceutical Equipment
Pharmaceutical Cleanroom Equipment
Cleanroom Contamination Testing Equipment
Cleanroom Contamination Testing Equipment
Detecting and mitigating contamination in pharmaceutical cleanrooms is instrumental in ensuring product safety and efficacy. Particulates and microbes can disperse at a fast rate, even radiating off a motionless person. Key purchasing considerations for cleanroom contamination testing equipment include the types of regulations followed in a pharmaceutical research or manufacturing facility, as well as the sanitary requirements for production of specific drug formulations.
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Axcess® MALDI-TOF for Microbiology Identification
Charles River
Sample Collection:
1 target plate with 96 spots
Glove Ports:
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Recirculated/Exhausted Air:
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HSC-40 Concentration System
Microbial-Vac Systems, Inc (MSI)
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Wet-Vacuum Surface Sampling
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Microbial-Vac System
Microbial-Vac Systems, Inc (MSI)
Sample Collection:
Wet-Vacuum Surface Sampling
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Microbial-Vac System with Support Equipment Case (SEC)
Microbial-Vac Systems, Inc (MSI)
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Wet-Vacuum Surface Sampling
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Articles
Facility Tour: Eurofins BioPharma Product Testing
AES Clean Technology Clients Celebrated with FOYA Awards
Contec Hosts Third Annual Cleanovators Virtual Summit
AES Clean Technology Accelerates Cleanroom Capabilities with $14.2 million Investment
Detecting Trace Elements in Single Cells with ICP-MS
Facility Tour: Eurofins BioPharma Product Testing -ATMP and Cell and Gene Therapy Testing Services for the Global Market
Cleaning, Disinfection and the Problems Caused by Chemical Residues
A Risk Assessment Approach to Address Fungal Spore Contamination in a Cell and Gene Therapy Cleanroom and Modern Methods for Control
FDA Takes Action to Restrict Unlawful Import of Xylazine
Azzur Group and Moderna Expand Business Relations
AdvantaPure Clean Room Expansion Completed
Contec® Hosts Second Cleanovators™ Virtual Summit
Potential Impact on Cleaning and Disinfection
Navigating the Complex Testing Strategies for Viral Vector-based Gene Therapies
Annex 1 and Cleaning Validation - How At-line and Online Analytical Methods Can Enhance Your Contamination Control Strategy
Executive Q&A: Aqueous Cleaning Handbook
Managing A Cleanroom Cleaning Team
The Value and Benefits of Rapid Mold Detection in the Pharmaceutical Industry
AES Clean Technology Expands Senior Leadership Team
Meeting the Evolving Need for Effective Nitrosamine Detection
FDA Seeks $7.2B to Enhance Food Safety and Nutrition, Advance Medical Product Safety, and Strengthen Public Health
Critical Behavioral Attributes and the Application of COM-B Framework in Aseptic Processing
FDA Takes Action Aimed at Helping to Ensure the Safety and Effectiveness of Laboratory Developed Tests
Report: Overall U.S. Product Recalls Reach Highest Quarterly Total In Past Five Years – Pharma Recalls Decline
The Challenges of Floor Cleaning and Sanitization
B. Braun Issues Recalls Sodium Chloride for Injection USP 1000 mL in E3 Containers Due to the Potential for Particulate Matter and Leakage
Flow Dynamics in Cleaning Applications
Don’t Stop Thinking About Tomorrow
Disinfect, Autoclave or Use Multiple-Bagged Disposables? Moving Materials into Controlled Areas Safely and Efficiently
Process Capability to Ensure Product Quality
Beyond the Cleanroom: The Human and Technological Edge in Aseptic Manufacturing
Comparing an Inspection by a Regulator to an Investigation by a Pharma Company
Nelson Labs to Double Cleanroom Capacity to Support Demand for Sterility Assurance Services
MicroQuant™ by ATCC
The Jar - Streamlining Critical Cleaning with New Packaging Solutions
Family Dollar Initiates Voluntary Recall of Certain Over-the-Counter Drugs and Medical Devices
Pharmaceutical P.I.N. Points: Patent Innovation News
Inspectional Readiness for Aseptic Cleanroom Operations
New Expectations for Training – Tied to Implementation of Contamination Control Strategies
Contamination Control Roundtable
All-in-one ICR Swab
Neutralizing Efficiency of Lecithin and Polysorbate 80 in ICR Contact Plates and Swabs for Surface Monitoring
Camber Pharmaceuticals Recalls Atovaquone Oral Suspension Due to Potential Bacillus cereus Contamination
Spectrum Labs Issues Voluntary Worldwide Recall of Epinephrine USP Bulk API Due to Discoloration of Product
FDA’s Updated Inspectional Approach in the Post-Pandemic Landscape
An Interview with Renee Morley, MBA
Facility Tour: Microbiologics - Expanding Infectious Disease Testing
Multidose Preservative-Free Container Closure Systems: Developmental Considerations for Sterile Small Molecule Drug Products
An interview with Niveen Mulholland, PhD - Vice President, Life Sciences, SGS North America
EMA’s Annex 1: Lead, Follow or Get Out of the Way
Report: Pharma Recalls Dropped in Q3 2024
Defining VHP Sterilization and Biodecontamination – Common Denominators and Differences
The Need for Speed and Confident Decision Making: Implementing Rapid Micro Methods (RMMs) Throughout Production
The Use of In-House Microbial Isolates in Disinfectant Efficacy Testing: Challenges and Solutions
Contamination Control Roundtable
AES Releases 3 New Standard Cleanroom Models
Minimizing Microbial Survival of Cleanroom Surfaces
A Guide to Developing an Effective Cleaning and Disinfection Program in Aseptic Environments
Maintaining Data Integrity During the Migration to Real-Time Testing
The Truth of Endotoxin Values - Points for Consideration During Investigation of Aberrant BET Results
INTERPHEX AWARD WINNERS 2023
Material World: Selecting Representative Surfaces for Disinfectant Compatibility and Efficacy Studies
Bacterial Spore Formers in Disinfectant Efficacy Testing
ForeverMen Supplements Recalled
Enhancing Material and Equipment Availability in Production Isolators
Haleon Issues Voluntary Nationwide Recall of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult Products Due to Microbial Contamination
Eagle - Experts in Sterility Testing
Cleanroom Disinfection: Maintaining Sterility by Design
Designing an Environmental Monitoring Solution for GMP Applications
USP <1111> Microbial Contamination Risk Factors Re-Visited
Endotoxin Testing Considerations – Reducing LAL Use with Compendial Methods
CIP Failures Due to Biofilm Formation: Strategies for Prevention and Remediation
How to Ensure Data Integrity When Digitalizing Your Microbial QC Lab Step by Step
The Sterility Testing Bottleneck and How Rapid Methods Can Overcome Them
Rapid Sterility Testing for Cell and Gene Therapy Treatments
Lack of Utility of the USP Tests for Specified Microorganisms
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