ComplianceOnline

This 3-hr Pharmaceutical Laboratory training will provide practical strategies for improving productivity in Pharmaceutical Laboratories, including hiring, training, establishing goals and approaches to lab automation and computerization.

Understand the requirements for investigations when dealing with pharmaceutical drug substances and products; to understand how to effectively control and conduct a laboratory investigation for unknown causes.

In this Bioanalytical methods validation understand the Clear, Consistent and compliant approaches for instrumental, ligand binding, and cell based methods.

This CLIA Laboratory Inspection training will discuss the salient features of laboratory inspection as per CLIA inspection guidelines.

This 4hr training will offer a lifecycle approach to assuring analytical methods are suitable for their intended use. It will detail the stages of an analytical method and provide practical suggestions.

This 8-hr webinar on Dissolution Methods for pharmaceutical dosage forms will provide you a comprehensive understanding of the development process and present a systematic approach for dissolution method development.

Learn how to differentiate and draw boundaries for GMP and GLP practices if done in same laboratory and how to transition a procedure in development to one used routinely.

This USP-1226 webinar training will discuss the requirements of USP-1226, what are FDA expectations related to method verification.

This Microbiology Laboratory training provide a comprehensive overview of the infrastructure of a compliant microbiology testing laboratory, preparation for an inspection, potential areas for nonconformance,test failures,resolution of audit findings.

Renowned speaker David Nettleton to train FDA regulated companies reduce costs associated with implementing, using, and maintaining computer systems in regulated environments.