Analytical Quality Control for the Pharmaceutical Industry

Analytical quality control refers to all those processes and procedures designed to ensure that the results of laboratory analysis are consistent, comparable, accurate and within specified limits. Quality control begins with sample collection and ends with the reporting of data. It is achieved through laboratory control of analytical performance.

This presentation will discuss Analytical Quality Control for pharmaceuticals as it relates to pipetting, weighing, sample collection and preparation, as well as analytical method and equipment qualification.

We will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. This presentation will help attendees understand the instrument qualification and system validation process and will provide instruction on how to prepare for audits and how to become FDA compliant.

Webinars will be available for unlimited on-demand viewing after live event.
 
LabRoots is approved as a provider of continuing education programs in the clinical laboratory sciences by the ASCLS P.A.C.E. ® Program. By attending this webinar, you can earn 1 Continuing Education credit once you have viewed the webinar in its entirety.