Pharmaceutical & Life Sciences

Pharmaceutical and life sciences facilities operate under intense regulatory scrutiny from the FDA, EPA, OSHA, and state agencies. EHS compliance intersects with Good Manufacturing Practice (GMP) in ways that require specialized understanding. Our auditors understand the unique challenges of pharmaceutical EHS: managing hazardous solvents and active pharmaceutical ingredients, maintaining cleanroom environmental controls, handling biological agents, managing pharmaceutical waste streams, and ensuring worker protection during potent compound manufacturing.

Pharmaceutical facilities face specialized EHS challenges: • Chemical exposure control for potent compounds and active ingredients • Pharmaceutical waste classification and disposal • Air emission controls including solvent recovery systems • Cleanroom environmental monitoring and validation • Laboratory safety and chemical hygiene program compliance • Biosafety requirements for biological materials Our ISO 14001 and ISO 45001 audits address these pharmaceutical-specific risks within the management system framework, ensuring your EHS programs are both compliant and effective.