Andrea Matter

Director, Regulatory Affairs at RPRD Diagnostics

Andrea leverages over a decade of experience in clinical diagnostics, specializing in CLIA/CAP compliance, quality management, and GMP documentation. She provides consultation to RPRD clients on all of their compliance needs, ranging from patient privacy (HIPPA) and safety for healthcare management to understanding FDA guidelines. Andrea understands that robust quality standards and continuous improvement are the keys to providing RPRD clients with superior pharmacogenomics results. Testing accuracy and patient safety is always her top priority.

Location

Milwaukee, United States

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RPRD Diagnostics

RPRD (Right Patient Right Drug) Diagnostics specializes in providing innovative pharmacogenomics solutions, including diagnostic, analysis and supporting services to clinicians, researchers and drug developers. With decades of experience in pharmacogenomics research, clinical practice, and healthcare program development, RPRD’s team of experts strives to improve patient lives using pharmacogenomics to enable precision medicine.


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11-50

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