PerkinElmer Genetics has a long history and is dedicated to improving the lives of families by offering early detection of inherited disorders. As one of the world’s largest providers of newborn screening services, we have decades of experience in screening for complex rare diseases. With over six million babies screened globally since 1994, PerkinElmer Genetics helps saves the lives of thousands of babies every year.
We are proud to continue the tradition by offering clinical genetic services to help provide a continuum of care for our patients and clinicians. PerkinElmer Genetics is now launching comprehensive genetic testing solutions that will help provide meaning into the complex nature of rare and inherited diseases.