Archived On Demand Webinars
Monitoring of nonviable and viable particles in a cleanroom is critical to meet regulatory requirements. An environmental monitoring system effectively collects, manages and reports on data from both types of sensors
Best known methods to minimize external contamination in the sample are presented to support data optimization. Customers are encouraged to incorporate these concepts in their own process development.
When designing a process, product quality is an important measure of success. To ensure product quality, it is imperative that the environment is monitored for contamination.
Control of the environment in which pharmaceutical products are manufactured is a key element of Good Manufacturing Practices (GMP). Monitoring of particles & microorganisms in manufacturing cleanrooms, Restricted-Access Barrier Systems (RABS), and isolators consists of clearly defined components.
Download this on demand webinar to get a first look and review of the Annex 1 draft, released for comments. Our experts will be providing their comments and will want to hear your thoughts on this new version.
Microbiologists have long recognized there are significant numbers of microorganisms in the environment that cannot be cultured successfully with conventional methods. A wide range of nonsporulating gram-negative and gram-positive bacteria can exist in the Viable But Non Culturable state.
Today, both the MHRA and FDA are highly focused on data integrity and currently discourage methods by which data is recorded manually.
ISO 21501-4 has two main goals; to improve instrument-to-instrument data correlation and count accuracy, and to enhance compliance with ISO 14644.
Learn about ISO 14644-2:2015 and how it affects your clean environment monitoring.
ISO 14644-2:2015 is not only a new standard with which to be compliant, but is also a beneficial tool to use in achieving mature cleanroom environmental control.
Attend this webinar to learn about the USP 1116 changes and how this impacts microbial control and monitoring in aseptic processing environments.
Learn about ISO 14644-1:2015 and how it affects your clean environment monitoring.
The recent revision of ISO 14644-1 introduced several changes for cleanroom classification and monitoring guidelines. Join us for a review of the changes and how they affect your environment monitoring.
Decreasing the time to detect, contain and mitigate very low levels of Airborne Molecular Contamination (AMC) is critical for high tech manufacturers.
Identifying the best rapid microbial monitoring solution for your critical & ISO 5/ Grade A surfaces
Managers need the assurance that the surfaces in their facilities are aseptic. Gaining that knowledge in a fast and accurate way that also provides results for all surfaces, even and uneven, is a challenge.
Personnel pose the greatest risk of false positives in aseptic processing. The BioCapt® Single-Use eliminates false positives and costly investigations by preventing direct operator contact with the media plate.
Learn about different options and considerations to protect your data integrity in an environmental monitoring system.
Quality by Design (QbD) is a well-known concept in the pharmaceutical industry to increase the overall quality of pharmaceutical drugs and increase patient’s safety. Controlling the quality of air inside an environmental monitoring program is a vital aspect of managing the risk towards the patient.
Advanced optics manufacturing now requires much cleaner environments than were necessary in the past. This webinar provides an overview of particle generation sources, control methods and ISO standards, to help you achieve a clean environment that maximizes productivity.