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.

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Our area of specialties includes:

For Clinicians

PerkinElmer Genetics is a global leader in providing screening and diagnostic testing for rare and inherited diseases. We are a provider who combines high-volume screening with diagnostic genetic testing.

For Patients and Parents

Patients and Parents suffering from complex rare genetic diseases often have limited places to turn for testing and treatments. PerkinElmer Genetics helps turn the complex nature of the disease into more understanding by providing meaningful and actionable genetic test results.

For Pharma

Our goal is to help pharmaceutical and biotech companies in successful drug development and commercialization by providing diagnostic testing solutions.
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