If you’re looking to strengthen USP <790> inspection practices, improve particulate detection, or ensure full 21 CFR Part 11–compliant documentation, a quick conversation can help you identify the right path forward. With extensive experience in pharmaceutical manufacturing, I support teams through both standard and custom inspection projects, tailoring solutions to fit existing clean room workflows and regulatory expectations.

Whether you need configurable software, purpose-built inspection equipment, or guidance on integrating new technology, my focus is providing high-level, responsive service that aligns with your operational needs.

Use my Calendly link below to schedule a meeting at your convenience, and let’s explore solutions designed specifically for your facility.