Committed to the pharmaceutical, biotechnology, cosmetic, contract and device industries, we provide regulatory-compliant process automation, legacy system migration, system integration, collaborative engineering, manufacturing, and other solutions for the supply chain.
Our validation services are designed to provide validation in accordance with all current GMPs, GLPs, GCPs, 21 CFR Part 11 (electronic records and signatures), PAT (Process Analytical Technologies), ISO and other global guidelines and regulations from the EU, United Kingdom, Japan, Singapore, Canada, and other regulations, as well as our client’s standards and expectations. Our knowledgeable consultants, project engineers and project managers have experience in applying the best business and validation practices.
We help you improve quality, reduce time to compliance, improve time to market, reduce operating costs and improve operational efficiency.
Our globally focused business unit has offices in North America, Europe and Asia Pacific with capabilities for local support of global validation projects.
