IV Room Design and Upgrades

We provide expert guidance in designing new sterile compounding facilities or upgrading existing IV rooms to meet current USP <797> and USP <800> standards. From initial planning to final execution, we ensure every detail is optimized for safety, compliance, and operational efficiency

Regulatory Compliance Support

Navigating complex regulatory requirements can be challenging. Our team helps you stay compliant with state, federal, and industry standards, including FDA and USP guidelines. We provide audits, gap analyses, and tailored action plans to ensure full compliance

Training and Education

We offer comprehensive training programs for your staff to ensure they understand and follow the best practices for sterile compounding. Our education sessions are designed to promote a culture of safety and excellence within your organization

Risk Management and Quality Assurance

Our experts identify potential risks in your compounding processes and implement robust quality assurance measures. From environmental monitoring to process validation, we help you build a foundation for long-term success.