Microbial Solutions Digital Resources

During these uncertain times, e-learning has never been more important. Our Microbial Solutions portfolio of digital resources is available on-demand to keep your endotoxin testing, microbial detection, and microbial identification education current.

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Articles

USP Chapter 1085: Frequently Asked Questions
Endotoxin Calculations: FAQ Document
Endotoxin Test Methods Comparison Sell Sheet
Putting Endotoxins to the Test
Mechanism of Low Endotoxin Recovery Caused by a Solution Containing a Chelating Agent and a Detergent 
Evaluation of LAL and Recombinant Endotoxin Alternative Assays for an Assessment of Endotoxin Detection Specificity
From the Ocean Floor to Outer Space
Fireflies & Horseshoe Crabs: Innovating Science
Testing the Tests for Contaminated Water


Blogs

Pharma 4.0 
Recombinant Factor C Under the Microscope
The Rapid-Fire World of Endotoxin Testing
Conquering Data Integrity By Eliminating Human Error 


Posters

Aspects of Mechanism in Low Endotoxin Recovery 
Utilizing Robotics to Increase LAL Testing Efficiency  


Webinars

What You Need to Know About USP <1085>
Understanding Glucan Impact on Endotoxin Testing
Hints and Tips for Ensuring a Successful LAL Product Validation
Make or Break Your LAL Assay: Choosing the Best Accessories for Your Endotoxin Testing Program
Keeping Quality Control, Bioburden Testing, and New Technologies Current with Annex 1 
Calculating Endotoxin Limits 
Data Integrity: Eliminating Risk & Human Error in Endotoxin Testing
Using Six Sigma Tools for Out of Specification (OOS) Investigations 
Transforming Analytical Data Into Actionable Results
LER: A Biopharmaceutical Operational Reality Perspective
Guidance for Evaluating and Investigating Endotoxin OOS/OOT and Atypical Results
Automating the Microbiology Laboratory: Past, Present, and Future
The Analytical Reality of Recombinant Endotoxin Technologies

Video

Nexus Demo Video

Articles

Accelerating Development and Release of mRNA-based Therapeutics to Market Using Rapid Methods
Implementation Strategies for Validating Alternative Methods
How to Select the Right Rapid Microbial Method


Blogs

What can Pharma QC Micro Learn from the Cosmetics Industry?  
Fireflies & Horseshoe Crabs: Innovating Science

 

Webinars

STAT Results for STAT Samples: Implementing Modern Rapid Micro Methods
Back to Basics: Environmental and Sterility Assurance Control for Medical Devices
Celsis® for Sterility Product Spotlight Webinar
Keeping Quality Control, Bioburden Testing, and New Technologies Current with Annex 1 
Celsis® For Sterility: Validating a 7-Day Direct Inoculation Sterility Test Using the Celsis Advance 
Celsis® For Sterility: Validating a 7-Day Membrane Filtration Sterility Test 
Rapid ATP-Bioluminescence for Non-sterile Product Testing: Roadmap to Implementation  

Posters

Demonstrating Equivalency and Limit of Detection for a Rapid Sterility Method using ATP-Bioluminescence
Rapid Microbial Detection In-Process Biomanufacturing Controls
Demonstrating Method Suitability for an ATP-bioluminescence Rapid Method for Egg-Based Vaccine Testing

Other Resources

Celsis Advance II™ Virtual Instrument Demonstration
Guidance on Implementation of Alternative and Rapid Microbiological Methods Ebook
ARMM Technology Comparison Worksheet
Accelerating Development and Release of mRNA-based Therapeutics to Market Using Rapid Methods Case Study
Extending Column Resin Life and Reducing Downstream Costs through Rapid Microbial Methods Case Study
Celsis AMPiScreen® Tested Products Fact Sheet

Articles

Fagron Sterile Services Relies on Charles River for Critical QC Testing 
Reducing Risk in Your Environmental Monitoring Program
Qualifying Your Cleanroom
Best Practices in the QC Micro Laboratory
Why should you care about Burkholderia cepacia?
Annex 1 Regulatory Changes Increase Expectations for Pharma
Filamenttous Fungi - Facilities Facing Facts

Blogs

Maintaining Quality and Environmental State-Of-Control
Microbiology Core Competencies and Control in the Facility
Annex 1: Regulatory Changes Increase Expectations for Pharma
Microbial ID in Quality Control Microbiology: An Industry Perspective
How Ready Are Your Cleanrooms for Annex 1 Updates?
The Key to Environmental Monitoring
Q&A with Ziva Abraham

Webinars

Environmental Monitoring and Cleanroom Qualification: What to Expect in the New Annex 1
Keeping Up with Annex 1 Revisions
Back to Basics: Environmental and Sterility Assurance Control for Medical Devices
Microbial Identification: How to Comply with the Current and Future Versions of USP Chapter <797>
A Bacillus cereus Situation: How New Species in the Group Can Affect Manufacturing
Microbial Identification Using A Phylogenetic Approach
Best Practices for Environmental Monitoring and Risk Management
Burkholderia cepacia Complex in the Pharmaceutical Industry
Reducing Manufacturing Risks with Molecular Identification Methods
Understanding the EU GMP Annex 1 Revisions
Tracking and Trending Made Easy
Optimizing MALDI-TOF for Filamentous Fungi Identification
Mold Contamination, Investigation, and Remediation Challenges
Keeping Up With Annex 1 Revisions: Impact of Major Changes
Environmental Monitoring and Cleanroom Qualification: What to Expect in the New Annex 1

ePosters

Data Integrity in the Microbiology Lab 
How Accurate and Robust is Your Fungal Characterization Strategy?
Comparing Sequence-Based Microbial Identification Methods
Operational Impact of Accurate Microbial Identification within the Burkholderia Cepacia Complex

 

Tools

What is your Microbial ID Program Really Costing You?