Guidance and implementation support for USP <797>, <800>, <823>, <825>, and FDA 503A/503B programs to ensure safe handling of sterile, non-sterile, hazardous, and radiopharmaceutical drugs.

Expert review and design planning for pharmacy cleanrooms, including workflow optimization, equipment selection, temporary facilities, and commissioning support.

Design of differential pressure control systems and development of environmental monitoring programs to minimize contamination risk and maintain sterile conditions.

Support for SOP development, staff training, and quality assurance practices based on proven best practices and regulatory expectations.

Support in responding to regulatory inquiries, managing downstream contamination risk, and integrating toxicology and occupational health expertise into pharmacy operations.