Summary : This live training webinar will also examine a variety of the issues surrounding microbial testing of raw materials. more...

Summary : Review of the new latitude within USP <61> and how it may impact OOT and OOS. Examine issues that may occur within the Incoming Raw Materials, In-Process and API phases. more...

Summary : The instructor-led training webinar is designed to assist in assuring that your organization is maintaining itself within a GMP compliance framework. "Real life examples", i.e., Form FDA 483s and Warning Letters will be used to illustrate specifics. more...

Summary : The objective of this live and interactive training webinar is to assist those involved in the development of a process or the manufacturing of a product to explore the microbiology of water, as a raw material in a GMP environment. more...

Summary : The World Congress on Microbiology takes place in Paris from February 21-23, 2019. Microbiologists from all over the World will meet to share the latest advancements in their field. more...

Summary : This course will also review the guidance provided in USP <1116> to ensure compliance with regulatory expectations are met. more...

Summary : Whether you are auditing a raw material supplier, a testing laboratory, or your own facilities, you should be aware of the critical role that microorganisms play throughout. more...

Summary : This live webinar will also explore the use of parametric techniques to permit product release without the requirement for the fourteen day sterility test. more...

Summary : The objective of this live training webinar is to explore the NEW/REVISED guidances for Industry on pyrogen and endotoxin testing addressing those issues that may be subject to misinterpretation. more...

Summary : The objective of this live training webinar is to obtain an enhanced understanding of the various USP microbial methods. more...

Summary : This live training webinar is for pharmaceutical, cosmetic, neutraceuticals and other industries that produce product not labeled as sterile.  Microbiological issues in non-sterile manufacturing and FDA regulatory expectations will be addressed. more...