This webinar is ideal for those purchasing or upgrading a LIMS. Learn the best way of building a business case for your LIMS, and how to get your LIMS project through the approval hoops in your organization and into reality.
This webinar is ideal for QC Laboratories involved in manufacturing processes that require clean/sterile conditions. Environmental Monitoring is used in the production of food/beverage, medical devices, and pharmaceuticals. It is the ideal solution to monitor repeat sampling in defined locations.
This webinar explores how a laboratory information management system (LIMS) provides a solid management framework for your laboratory. Learn about the core functions you should expect in a LIMS and modules you can add to maximize efficiency and improve results in your laboratory.
Within any batch manufacturing environment whether in highly regulated industries such as pharmaceutical and medical devices or not, there exists an array of systems that create, manage and distribute the data vital to the manufacturing process. This webinar will cover the role of Laboratory Information Management Systems (LIMS) within this environment and explain why it is a key element in ensuring the quality of your products and in protecting your reputation.
The ideal webinar for anyone considering or starting a LIMS project in 2021. Learn the steps you should take to ensure your LIMS project is a success. Discover how to best gather your internal “User Requirements”, find out what you need to know from your Laboratory team and what questions to ask potential LIMS vendors.
How do you make the laboratory a key component of your business? A LIMS should be the hub of your operation, not only managing your data, but also growing and protecting your business, and increasing your profits.
Are you interested in learning the secrets of LIMS configuration to allow easier modifications, extensions and upgrades? How can you ensure your implementation is successful? All laboratories are different, and therefore LIMS need to be configured to meet differing needs, as well as to be regularly updated to ensure long-term success.
LIMS Validation is a buzzword that tends to be widely misunderstood, and much abused, in the laboratory industry. And yet it is an important and challenging task. The US Food and Drug Administration (FDA), equivalent worldwide regulatory bodies and many certification bodies such as ISO, require that software systems be tested and proven to work as intended. LIMS validation is therefore a vital step in regulated environments, certified laboratories, and best practice laboratories to ensure data integrity and prove compliance. In this webinar, we will discuss what system validation involves and explain how you can achieve the validation of your LIMS system.
Find out how we can help maximize efficiency and minimize risk for your laboratory.
