Facing the Challenge: Practical Approaches to Evaluate Analytical Performance

This series of three live Web broadcasts, co-sponsored by the National Laboratory Training Network (NLTN), will describe how to use Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) documents to establish and monitor the analytical performance of laboratory assays. This valuable information will help professionals in laboratories and/or manufacturers:

• meet regulatory laboratory performance requirements;
• satisfy regulatory requirements for establishing performance claims for in vitro diagnostic assays; and
• validate manufacturers’ performance claims.

Each of the three live broadcasts will include expert presentations with accompanying handout materials and a Q&A session with Webcast speakers who are thought-leaders representing laboratory, government, and industry perspectives.

• Invite your entire staff to participate. Site registration has no limit on the number of attendees.
• Obtain 1.5 PACE ® continuing education credits per session.
• Subscribe to each session individually ($195 each) or purchase all three for additional savings ($499 total).

12 June at 1:00 – 2:30 p.m. ET:  TO REGISTER
* How CLSI Documents Fit Into a Quality Management System
* Overview of FDA’s Perspective on CLSI Evaluation Protocols (EP) Documents

26 June at 1:00 – 2:30 p.m. ET:  TO REGISTER
* Use of CLSI Evaluation Protocols (EP) to Establish Performance Claims for In Vitro Medical Devices
* CLIA QC and CLSI Evaluation Protocols Documents

10 July at 1:00 – 2:30 p.m. ET:  TO REGISTER
* Using CLSI Evaluation Protocols (EP) to Validate Assay Performance in the Laboratory
* Manufacturer Validation and Laboratory Utilization of QC Protocols
* The European IVD Directive – What Does It Mean to Me?

SAVE
Register for all three Web broadcasts for one discounted price. [ return to top ]