Adopting an Electronic Document Management System (EDMS) for HSE constraints. Legitimizing digital signatures and automating logs. Drops the overwhelming bureaucratic burden on HSE specialists preventing legal loss.
Integration of HSE management system processes into the pharmaceutical quality system. The practice includes combining HSE instructions with Standard Operating Procedures (SOPs), conducting joint audits by quality and HSE departments, and including safety issues in risk analysis during production changes and incoming raw material control.
Transition to a new HSE management model based on process and risk-oriented approaches. Implementation of occupational risk assessment at each workplace, followed by documenting the results in local regulations and HSE instructions.