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Pharmaceutical Equipment
Pharmaceutical Cleanroom Equipment
Cleanroom Contamination Testing Equipment
Cleanroom Contamination Testing Equipment
Detecting and mitigating contamination is pharmaceutical cleanrooms is instrumental in ensuring product safety and efficacy. Particulates and microbes can disperse at a fast rate, even radiating off of 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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HSC-40 Concentration System
Microbial-Vac Systems, Inc (MSI)
Sample Collection:
Wet-Vacuum Surface Sampling
Glove Ports:
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Microbial-Vac System
Microbial-Vac Systems, Inc (MSI)
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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
Detecting Trace Elements in Single Cells with ICP-MS
Cleaning, Disinfection and the Problems Caused by Chemical Residues
Potential Impact on Cleaning and Disinfection
The Value and Benefits of Rapid Mold Detection in the Pharmaceutical Industry
Navigating the Complex Testing Strategies for Viral Vector-based Gene Therapies
AES Clean Technology Expands Senior Leadership Team
On-Demand Webinar: Building Cleanrooms At Warp Speed
AdvantaPure Clean Room Expansion Completed
AES Clean Technology Accelerates Cleanroom Capabilities with $14.2 million Investment
A Risk Assessment Approach to Address Fungal Spore Contamination in a Cell and Gene Therapy Cleanroom and Modern Methods for Control
FDA Seeks $7.2B to Enhance Food Safety and Nutrition, Advance Medical Product Safety, and Strengthen Public Health
Facility Tour: Eurofins BioPharma Product Testing -ATMP and Cell and Gene Therapy Testing Services for the Global Market
Annex 1 and Cleaning Validation - How At-line and Online Analytical Methods Can Enhance Your Contamination Control Strategy
Azzur Group and Moderna Expand Business Relations
Contec® Hosts Second Cleanovators™ Virtual Summit
Managing A Cleanroom Cleaning Team
Brochure: Annex 1 Ready — Reliable, Confident Environmental Monitoring
Meeting the Evolving Need for Effective Nitrosamine Detection
FDA Takes Action to Restrict Unlawful Import of Xylazine
Executive Q&A: Aqueous Cleaning Handbook
All-in-one ICR Swab
New Expectations for Training – Tied to Implementation of Contamination Control Strategies
Contamination Control Roundtable
Pharmaceutical P.I.N. Points: Patent Innovation News
Neutralizing Efficiency of Lecithin and Polysorbate 80 in ICR Contact Plates and Swabs for Surface Monitoring
FDA’s Updated Inspectional Approach in the Post-Pandemic Landscape
The Jar - Streamlining Critical Cleaning with New Packaging Solutions
Family Dollar Initiates Voluntary Recall of Certain Over-the-Counter Drugs and Medical Devices
Inspectional Readiness for Aseptic Cleanroom Operations
Spectrum Labs Issues Voluntary Worldwide Recall of Epinephrine USP Bulk API Due to Discoloration of Product
Camber Pharmaceuticals Recalls Atovaquone Oral Suspension Due to Potential Bacillus cereus Contamination
An Interview with Renee Morley, MBA
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
Facility Tour: Microbiologics - Expanding Infectious Disease Testing
Contamination Control Roundtable
AES Releases 3 New Standard Cleanroom Models
The Use of In-House Microbial Isolates in Disinfectant Efficacy Testing: Challenges and Solutions
The Need for Speed and Confident Decision Making: Implementing Rapid Micro Methods (RMMs) Throughout Production
Bacterial Spore Formers in Disinfectant Efficacy Testing
INTERPHEX AWARD WINNERS 2023
A Guide to Developing an Effective Cleaning and Disinfection Program in Aseptic Environments
Maintaining Data Integrity During the Migration to Real-Time Testing
Material World: Selecting Representative Surfaces for Disinfectant Compatibility and Efficacy Studies
Minimizing Microbial Survival of Cleanroom Surfaces
The Truth of Endotoxin Values - Points for Consideration During Investigation of Aberrant BET Results
ForeverMen Supplements Recalled
Haleon Issues Voluntary Nationwide Recall of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult Products Due to Microbial Contamination
Designing an Environmental Monitoring Solution for GMP Applications
USP <1111> Microbial Contamination Risk Factors Re-Visited
Enhancing Material and Equipment Availability in Production Isolators
Endotoxin Testing Considerations – Reducing LAL Use with Compendial Methods
The Sterility Testing Bottleneck and How Rapid Methods Can Overcome Them
Rapid Sterility Testing for Cell and Gene Therapy Treatments
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