Our Services

Comprehensive routine and terminal cleaning services for sterile compounding environments. Our team performs the detailed cleaning required to maintain controlled environments while reducing the workload placed on pharmacy personnel. For organizations that perform cleaning internally, we also provide hands-on training and competency validation for pharmacy, environmental services (EVS), and other designated personnel responsible for cleanroom cleaning.

From PECs and cleanroom surfaces to floors, walls, ceilings, shelving, and equipment, our services are designed around the unique requirements of sterile compounding environments. We use appropriate cleaning agents, techniques, frequencies, and documentation practices to support alignment with USP <797>, USP <800>, manufacturer instructions, and facility-specific requirements.

Whether you need ongoing cleaning support, assistance with terminal cleaning, or help developing and validating an internal cleaning program, PurePath provides practical solutions designed to promote consistency, compliance, and survey readiness.

Including:

• Routine and terminal cleanroom cleaning

• PEC, buffer room, anteroom, and controlled area cleaning

• Cleaning of ceilings, walls, floors, pass-throughs, shelving, and equipment exteriors

• Sporicidal, disinfectant, and sterile IPA cleaning programs

• Hazardous drug cleanroom cleaning services

• Cleaning procedures, documentation, and audit-ready logs

• Hands-on cleanroom cleaning training for pharmacy, EVS, and designated personnel

• Cleaning technique observation and competency validation

• Customized cleaning programs based on facility design, equipment, and workflow

Expert regulatory consultation designed to help organizations achieve and maintain compliance while optimizing sterile compounding operations. Our team partners with yours to identify compliance gaps, evaluate workflows, assess risk, and develop practical solutions that support long-term operational success and inspection readiness.

Whether you're preparing for an accreditation survey, implementing new standards, responding to regulatory findings, or seeking guidance on best practices, we provide tailored recommendations and hands-on support to meet your organization's needs.

Services include:

• Mock Joint Commission and regulatory readiness assessments

• USP <797> and USP <800> compliance evaluations

• Gap analyses and risk assessments

• Corrective action plans and implementation support

• Policy and procedure review

• Workflow optimization and operational recommendations

• Virtual and on-site consultation

• Ongoing compliance support and regulatory guidance

Guided review of policies, standard operating procedures (SOPs), and supporting documentation designed to promote safe, compliant, and standardized sterile compounding practices. We work closely with your organization to ensure practical, easy-to-follow resources that align with USP standards, accreditation requirements, and your operational workflows.

Whether you're building a new program, updating existing documentation, or standardizing processes across multiple locations we ensure documents are clear, sustainable, and audit-ready.

Including:

• Standard operating procedures (SOPs)

• Policies and programs

• Work instructions and quick reference guides

• Training materials and visual job aids

• Forms, logs, and audit templates

• Custom project support upon request

Comprehensive competency assessment and validation services designed to support compliance with USP <797> and USP <800> requirements while promoting safe, consistent sterile compounding practices. We partner with your organization to provide standardized, hands-on competency evaluations that assess both knowledge and demonstrated performance.

Whether you're establishing a new competency program, supporting initial qualification, completing required recurring assessments, or standardizing competency practices across multiple locations, PurePath provides a structured and practical approach with clear documentation to support ongoing compliance and survey readiness.

Including:

• Initial USP <797> competency assessment and validation

• Semi-annual USP <797> competency assessment and validation

• Annual USP <800> hazardous drug competency assessment and validation

• Hand hygiene and garbing competency

• Aseptic manipulation and compounding technique

• Gloved fingertip and thumb sampling

• Media-fill testing

• Hazardous drug handling, PPE, and compounding practices

• Competency documentation and completion records

• Customized competency support based on facility practices and equipment