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...
Browse Content
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...
Data Integrity in the Age of AI: Securing Connected Devices
As artificial intelligence becomes increasingly embedded in medical devices and healthcare systems, the concept of data integrity...
Fundamentals of Disinfectant Efficacy
Disinfectants must be qualified on the surfaces present within a pharmaceutical manufacturing environment before they are approved...
Navigating the Decision Flow: Changing Sterilization Modalities for Medical Devices
As global regulatory pressures tighten and supply chain challenges increase, medical device manufacturers are increasingly considering changes...
Integrated Approach for Bulk Pharmaceutical Sterilization
Our popular Capsule Learning Webinars are back! All of the expertise of a webinar in 30 minutes...
Radiation Sterilization: What do product characteristics tell you about the type and source of radiation to use?
Since the installation of the first irradiators for the sterilization of single-use healthcare products in the 1960’s,...
Benefits of Parametric Release for EO Sterilization
Introducing Capsule Learning from Sterigenics. All the expertise of a webinar in 30 minutes or less. Join...