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...
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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...
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...
Contamination Control for Pharmaceutical Products Real World Moist Heat Validation Pitfalls and Proper Verification of Sterility
Moist-heat sterilization is a commonly used and widely accepted process in pharmaceutical manufacturing. Given its critical role,...
Overcoming a Cytotoxicity Failure
Every medical device must demonstrate proven biocompatibility to protect users from potential biological risks associated with its...
Biocompatibility Essentials
Biocompatibility is a crucial aspect of medical device design and manufacturing, ensuring that devices do not cause...