Environmental contamination control is a crucial aspect of sterile pharmaceutical manufacturing, and risk management is needed to guarantee that the necessary control procedures are in place. The risk ...

Chemical regulations exist to safeguard human and environmental health throughout a substance’s life cycle (manufacture, intended use phase, and disposal). Regulatory decisions require scientific ...

Annually, we perform a campus wide risk assessment, with the support of Internal Audit and the University’s Compliance Program. We embraces a holistic strategy for risk identification, utilizing a ...

This session will review and describe the basic steps of a biosafety risk assessment for clinical laboratories. The risk of exposure to infectious agents exists in every clinical laboratory.

How auditors assess and respond to risks of material misstatement in the financial statements, including the risk of fraud, is a critical component of audit quality. New research supported by the ...

The process used by EPA to evaluate the safety of chemicals needs to be streamlined to ensure that risk assessments use appropriate scientific data and are relevant to decisionmakers, concludes a ...

Once the risk team has been assembled, the crucial process of identifying risks must commence. The output of the risk ...

BOSTON & DENVER--(BUSINESS WIRE)--ProcessUnity and CyberGRX announced today that the Third-Party Risk Management (TPRM) leaders have joined forces, creating the industry’s most powerful software and ...

Eight standards rolled out in 2006 by the Auditing Standards Board are sparking a cultural shift for auditors. The standards—Statement on Auditing Standards nos. 104–111—are designed to enhance ...

Conducting a comprehensive security assessment is imperative to ensure that all of a campus’ possible weak spots and entry points are addressed. By conducting a risk assessment, campus administrators ...