Bioburden Testing and Microorganism Characterisization: Enhanced Guidance for Low Sterilization Dose Products
In recent years, concerns have been raised regarding the lack of understanding of bioburden (both numbers and...
Archives: Courses
Understanding Radiation Methods of Dose Establishments and Importance of Sterilization Dose Audits
Join us for this popular webinar as we delve into the various methods used to establish the...
Introduction to Industrial Sterilization
Join us for an insightful presentation featuring expert advisors Erik Hagedooren, Senior Director of New Sterilization Technologies,...
2023 Spring AAMI Standards Week Update
In this podcast from Nelson Labs, business leaders who recently returned from the AAMI standards week meetings...
Introduction to Microbiology and Sterilization
Are you looking for foundational knowledge on microbiology as it relates to sterilization services and testing? Watch...
Removing rabbits from irritation testing: Current status of regulatory acceptance of ISO 10993-23
In recent years, significant changes have been made to the standards and practices surrounding biocompatibility testing, driven...
Skin Care Products Understanding Clinical Testing Options
Skin-care products have become an essential part of the cosmetic and personal-care industry. Whether you are dealing...
Is it time to Re-Evaluate your Design History File for Reusable Device Validations
Standards for reprocessing have become a top priority for regulatory bodies worldwide. The active work around reusable...
Guidance on Combining Biocompatibility and Cleaning Validation Testing
Testing all biocompatibility endpoints for reusable medical devices both at first-time use and after multiple reprocessing cycles...
The Biocomp Trail A Challenging hike towards Animal Free Testing
The main purpose of ISO 10993-1 is to emphasize a risk-based approach for evaluating the biocompatibility of...
Appropriate uses for Product Sterility Testing When is Sterility testing appropriate
Sterility testing is often the first test that comes to mind when determining if something is “sterile.”...
EPA Regulatory and Testing Guidelines for Residual Efficacy
With the recent implementation of the EPA guidance for residual efficacy claims on antimicrobial products, there is...
Release and Stability Testing Requirements for Parenteral Drug Products
Parenteral products, which include sterile drugs, solutions, emulsions, and suspensions, are distinct from other pharmaceutical dosage forms...
Introduction to Evaluating Persistent or Residual Antimicrobial Efficacy of Topically Applied Products
Topically applied antimicrobial products are vital tools in limiting the spread of microorganisms and diseases. These products...
The Impact of Radiation Sterilization Modalities on Flexible Sterile Barrier Packaging
Selecting the appropriate sterilization technology for your product and organization involves numerous factors. In this informative webinar,...
Understanding Container Closure Integrity Test Failures
Does a container closure integrity test (CCIT) failure always indicate a defective closure? This webinar aims to...
Medical Device BioFilms Slimy Sticky Stubborn and Serious
Major advances in medical devices over the last few decades have significantly improved the quality of life...
Evaluating Packaging Changes
Supply chain disruptions have made it imperative for businesses to rethink their supply chain management strategies. Incorporating...
Pros Cons and Considerations of Using a Developmental Chamber During Ethylene Oxide Validation
A developmental chamber, typically smaller than a production chamber, is often utilized to perform studies that support...
Slimy Biofilms A Brief Overview
A biofilm is a community of microorganisms embedded in a slimy matrix that can attach to a...