Take a moment to learn about our offerings and let us know how we can best alleviate any regulatory and documentation needs for your organization.
Our goal is to aid in growing CLIA and CAP certified laboratories throughout the United States by elevating the standards held by clinical laboratories. We pride ourselves in our attention to detail, high standards for clinical assay validations, extensive knowledge in CLIA/CAP compliance, SOP creation, document control implementation, document control maintenance, reviewing and implementing quality management programs, impartial advice, and practical assistance to help your laboratory make the most of every opportunity.
Is your laboratory experiencing growth and diversification? Let us help you develop your document control program, review your quality management systems, and quell any anxieties associated with expanding your testing capability. Our team will conduct detailed audits of your current documentation, forms, validations, and procedures to ensure that they are of the highest quality. Allow us to help you to reach new heights of analytical excellence.
Our laboratory experts thrive on elevating the standards for laboratories across the United States. We have experience in implementing a myriad of laboratory services including document control programs, CLIA waived blood testing, LIS implementation, semi-quantitative PCR assays, sanger sequencing based assays, custom oligomer design, in-house PT implementation, laboratory competency assessments, and regulatory compliance.
Our background is in clinical laboratory science, and we have aided in the development and implementation of a plethora of laboratory services. If you are experiencing growing pains, let us help you build a sturdy foundation to continue to thrive. Help us to understand what need we can fill in your organization so we can support growth, limit turnover rates, and help you to break through any barriers you may be experiencing while growing your testing menu. We also specialize in the conversion of qualitative qPCR assays to semi-quantitative assays.
Our consultation services include comprehensive evaluation of laboratory procedures which allow us to identify gaps in laboratory knowledge, comprehensive document control procedures, standard operating procedure generation, and guidance for laboratory validation procedures. We also offer remote laboratory support for the evaluation of validation data, validation report writing, assay design, and we are more than happy to travel to your site for an internal inspection to see what gaps need to be filled before your next inspection.
We will do everything in our power to provide your organization with the tools required to thrive in today's regulatory landscape. Whether you are looking to employ semi-quantitative qPCR assays, reinvent your document control program, or sooth a pain that is specific to your organization, call us today. Together, we will build a strong foundation for your organization to grow and exceed regulatory requirements without seeing detrimental impacts to your bottom line.
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