Real-time PCR, also known as quantitative PCR (qPCR), is the gold-standard for sensitive, specific detection and quantification of nucleic acid targets. This technology allows for powerful assay design algorithms, optimized master mixes, intuitive data analysis software, and diverse applications. The Analytical Validation of qPCR assays can, however, be a complex and time-consuming task.
In this webinar we will explore the need for the Analytical Validation (AV) and dive into what it takes to complete a qPCR AV. An experienced AV Project Manager will share their insight into the AV journey focusing on the most accepted validation guidelines, challenges and solutions for a successful Analytical Validation.
• Outline the principal validation guidelines
• Discuss the challenges that come with an Analytical Validation
• Discover Thermo Fisher Scientific’s approach to consulting on an AV project