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Roche NimbleGen commits to GMP and FDA submission for microarrays

The implementation of GMP will cover the full scope of processes from development through manufacturing
Written byJeffrey Bouley
| 2 min read

MADISON, Wis.—As part of assuring both quality and compliance, and with an eye toward future development and marketing needs, Roche NimbleGen has announced a company-wide initiative to implement good manufacturing processes (GMP) for its suite of DNA microarrays.

The implementation of GMP will cover the full scope of processes from development through manufacturing, it will include all locations, and it is intended as a step toward a subsequent submission to the U.S. Food and Drug Administration for clearance or approval of select array products.

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