Science Researcher Update: Spotlight on Meetings, Conferences, and Events
Spotlight on Science Meetings, Conferences and Events brings you information on the following event: Verification of Compendial methods: Discussion of the verification of compendial methods when introduced in a laboratory.
This webinar will discuss test method varification and what should be considered for the method verification process. The firm must demonstrate that the receiving laboratory is capable of performing the test and that the test results accurately reflect the attribute being tested.Read More
Spotlight on Science Meetings, Conferences and Events brings you information on the following event: Explore Scilligence Inventory for sample Management and Safety ComplianceRead More
Spotlight on Science Meetings, Conferences and Events brings you information on the following:What is MACRA and how does HIPAA apply?Read More
Spotlight on Science Meetings, Conferences and Events brings you information on the following event:Fixed Dose Combination Products. The Promise and PossibilitiesRead More
Spotlight on Science Meetings, Conferences and Events brings you information on the following event:Terminally ill Patients and the ‘Right to Try’: Practical, Legal, and Ethical Issues in Expanded Access to Investigational DrugsRead More
Spotlight on Science Meetings, Conferences and Events brings you information on the following event:Compliance Global 2017 FDA Regulation, 3D Printing and Medical DevicesRead More
In this webinar, the steam sterilization mechanism will be described as it relates to bacterial cells and endospores. The process and key terminology are defined. Understanding these fundamentals is critical to develop a successful autoclave sterilization process.
Why Should You Attend:
Successful autoclave Performance Qualification starts with a fundamental understanding of steam sterilization microbiology.
The webinar will lay out parameters of the sterilization process on a basis for conducting autoclave performance qualification studies. There are specific expectations for steam sterilization that must be met, whether it is continuing maintenance of existing equipment or qualifying a new autoclave installation. The session will also provide regulatory references on use of air removal verification tools, chemical indicators and biological, along with definitions for sterility assurance level, accumulated lethality, temperature mapping and biological verification.
Common questions and hot topics in industry will be presented to demonstrate the practical application of understanding steam sterilization. These points exemplify how the knowledge allows for efficient troubleshooting of unexpected events and for improving processes in an autoclave. Our expert will discuss the practical application of steam sterilization, address common questions, and cover industry hot topics. This knowledge will help professionals in efficient troubleshooting of unexpected events and for improving processes in an autoclave.
Areas Covered in the Webinar:
•Steam sterilization on a microbial level
•Autoclave Performance Qualification expectations
•Regulatory and GMP requirements for steam sterilization
•Process verification tools for use in an autoclave
•Common questions, problems and cGMPs
Who Will Benefit:
•Quality Assurance Managers
•Sterility Assurance personnel
- This FDA documentation webinar will explain the regulatory expectations for, and the proper design and maintenance of effective and compliant standard operating procedures (SOPs).
Webinar - Online
This 60-minute webinar will show how you can design a robust microbiological audit program for pharmaceutical and biopharmaceutical product manufacturing, that effectively assesses your facility and that of your supplier to ensure your facilities and products are free from microbial contamination.Read More