Always Inspection Ready: Mastering FDA Inspection Preparation and Response
With the FDA increasing unannounced and remote inspections, continuous inspection readiness is more important than ever. This...
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Understanding PDA/ANSI Standard 06-2025: A Roadmap for Culture Change
A robust quality culture is no longer a nice to have—it’s a regulatory and operational imperative. Watch...
Ensuring Drug–Device Compatibility: Foundations for Safe and Effective Combination Products
As combination products continue to advance healthcare, ensuring compatibility between drug formulations and device components is essential...
Fundamentals of Disinfectant Efficacy
Disinfectants must be qualified on the surfaces present within a pharmaceutical manufacturing environment before they are approved...
Integrated Approach for Bulk Pharmaceutical Sterilization
Our popular Capsule Learning Webinars are back! All of the expertise of a webinar in 30 minutes...
Nitrogen Dioxide: Innovative Gas Solutions for Healthcare Products
Finding the appropriate sterilization modality for your product requires an understanding of the options. Nitrogen Dioxide is...
Prefilled Ophthalmic Syringes New Possibilities in Terminal Sterilization
In this joint webinar, Eric Offermann and Bernd Zeiss speak about Nitrogen Dioxide (NO2) as a new...
Disinfectant Efficacy Testing on Site Specific Surfaces
Disinfection efficacy studies play a significant role in the Pharmaceutical manufacturing environment in ensuring that the surfaces...
Container Closure Integrity Testing for Pharmaceutical Sterile Barrier Packaging
Container Closure Integrity Testing (CCIT) is crucial for evaluating the sterile barrier integrity of pharmaceutical packaging, including...
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...