The revised TR significantly expands on the original 2000 document, providing enhanced guidance on validation, regulatory expectations, return on investment, scientific principles and implementation.
Please visit https://store.pda.org/ProductCatalog/Product.aspx?ID=2094 to access the TR.
If you are attending the PDA Global Conference on Pharmaceutical Microbiology in Bethesda next week, please join me on Tuesday from 11:00-11:30 am, where I will present an overview of the new TR.
If you cannot attend the PDA Micro meeting, I will be hosting a comprehensive 90-minute web seminar that will provide attendees with an overview of the new TR33 and a practical understanding of how to apply the guidance when validating and implementing rapid methods in their own facilities. Attendees will also have an opportunity to ask questions about TR33 or any other topic associated with RMMs. The webinar will take place on Wednesday, November 6 at two separate times to accommodate most geographic locations. Please register for this webinar at http://rapidmicromethods.com/events/November-6-2013-webinar-TR33-registration.php.