Roche announced today that its Roche Digital Pathology Dx slide scanner, the VENTANA DP 200, has received FDA 510(k) clearance. This system enhances pathology by enabling pathologists to review and interpret digital images of scanned slides, facilitating quicker diagnoses from any location.
Jill German, Roche Diagnostics' Head of Pathology Lab, highlighted that digital pathology streamlines workflows, enhancing lab efficiency and extending pathologists' reach to remote areas. Collaboration among pathologists is also bolstered, improving diagnostic accuracy and patient care.
Digital pathology transforms traditional histopathology by digitizing slide scanning, visualization, and analysis processes. Once tissue slides are scanned and converted into digital images, they can be shared and analyzed by pathologists. This capability aids in determining optimal treatments for cancer patients and supports more thorough analyses than traditional methods.
Roche is committed to advancing digital pathology through innovations like AI-based tools and its Roche Digital Pathology Open Environment. These initiatives aim to drive adoption and foster innovation in pathology.
Founded in 1896 in Basel, Switzerland, Roche has evolved into a global biotechnology leader and a pioneer in personalized healthcare and diagnostics. The company's dedication to scientific excellence and sustainability has been recognized consistently, including its long-standing presence in the Dow Jones Sustainability Indices.
Roche continues to invest in shaping the future of pathology by integrating research-oriented tools into routine clinical practices, thereby improving global healthcare delivery.