Clinical & Laboratory

  • A Highly regarded talk during recently held ASQ World Conference on Quality and Improvement. This course is meant to be a needed introduction to risk management for a broader range of professionals. Risk Elimination. Risk Management. Risk Mitigation. These...
  • Effective documentation of analytical procedures is essential to ensure that testing required by regulatory agencies is performed correctly and consistently. This webinar will cover some of the common mistakes made while writing analytical procedures, and will give examples of...
  • CarolynTroiano
    Organizations governed by FDA must adhere to strict requirements relative to data being captured, analyzed, reported or stored on computer systems. As such, organizations must be able to manage the data effectively, realize value from it, minimize the cost,...
  • “Good documentation practices” is a “current” industry practice that is reviewed and cited by federal regulators when audited. Pharmaceutical/Biological document are legal documents that are controlled by all regulatory agencies. The person or persons responsible for filling out these...