I specialize in providing remote document support for pharmaceutical commissioning, qualification, and validation documents. My services include creating traceability matrices, and summary reports, and offering authoring review services and validation master plans. These documents are developed using client-provided templates, reference materials, and critical process parameters (CPP), ensuring they meet data integrity requirements. With my extensive experience, I tailor each service to meet the unique needs of your facility, ensuring compliance with both regulated and non-regulated industry standards.
My time in leadership roles has provided me with a unique perspective and skill set that I bring to every project. I am dedicated to helping pharmaceutical companies navigate the complex world of regulatory compliance and documentation.
My remote support services are designed to be flexible and efficient, allowing you to focus on your core operations while I handle the documentation. Whether you need support for facilities, utilities, systems, or equipment, I have the expertise to ensure your documentation is accurate and compliant. Discover how my expertise can help streamline your documentation process and enhance your quality assurance efforts.