Using the Lab Information Management System (LIMS) in a Stability Testing Program

Who Should Attend
This webinar will provide a great resource to the Pharmaceutical, Biotechnology, Biologics, Drugs, Medical Device, In-vitro Diagnostics product manufacturers with personnel in the following functions: Quality Control, Quality Assurance, Stability, Microbiologist, Chemist, Analysts, Manufacturing, Validation, Materials Management, Regulatory Affairs and all levels of Management.

However, if you are already familiar with how to integrate and use a Lab Information Management System (LIMS) in a Stability testing program, you may recommend this webinar to professionals within the various industries that may require additional knowledge about this subject.

Description
This course will be available On Demand: August 30, 2013

This webinar will describe how to integrate, evaluate, manage, extrapolate, trend and use the data that is generated from a products’ stability testing program using the Lab Information Management system (LIMS). The LIMS can be effectively used to provide a meaningful, compliant and justifiable shelf-life/expiration date to a product when compared with a paper based or excel calculation that may sometimes not be easily validated.

This 90-minute accredited training course will allow the attendee to understand the step-by-step process of identifying and using the results of a product’s stability test data very effectively using the LIMS. The advantages/disadvantages of using manual or automated process, types of automated systems, how to choose the best Stability Testing LIMS program/module, guidance on how to perform data trending and effectively use the trend result in generating the final stability report will be discussed.