We have extensive expertise in scientific Quality Control, Quality Assurance, and Quality Management operation in an FDA-regulated pharmaceutical environment, and that experience and quality mindset permeates all we do at Robertson Microlit. We take extra care to minimize errors, understand your objectives, and work with you to meet your expectations.
When you submit your samples or projects to Robertson Microlit Laboratories, you can be assured that our entire staff understands that you expect competent, thorough, and expert handling of your analytical requests. In January 2024, FDA investigators carried out a general GMP inspection of our laboratories. As a result of that inspection, and as evidence of our strong Commitment to Quality, Robertson Microlit Laboratories received no Form FDA-483 observations.
We strive for seamless interactions and a collaborative relationship with each of our clients to effectively function as an extension of your own organization. Our management, quality, and professional staff are always available to you should you have any questions about our services, capabilities, or analytical procedures and results. Our goal is to rise above what you would expect from a service provider – and deliver a scientifically sound and reliable product every time.