Quality Documentation
With our Regulatory Health Check toolkit, we can provide documentation to help you maintain strict regulatory compliance
Meeting USP 797 Regulatory Guidelines
Through our three-step assessment, design, and implementation process, PHS can identify what’s necessary to comply with USP 797.
Assess
Pharmacy consultants review your operations, processes, and procedures; equipment monitoring; and clean room practices to determine your current compliance with the USP 797 regulations.
Design
Then, we develop an action plan, including the evaluation of equipment procurement and the review and updating of existing policies and procedures.
Implementation
Next, we outline a proposed training program and implementation plan to meet USP 797 standards, as well as a quality assurance plan for maintaining the clean room. Should new construction be a necessary step toward compliance, PHS can work with you to design and build a clean room, including assistance with space configuration, equipment placement, and storage area design.