EtQ for Life Sciences

In the Life Sciences industry, only the most innovative and cost-eff ective products will survive. Success in this industry requires adherence to applicable Food and Drug Administration (FDA) regulations (including 21 CFR 820 and 21 CFR Part 11), and may also involve meeting ISO standard requirements (such as ISO 13485). Rapid product development processes that are responsive to changing market demands are key to meeting the needs of this industry.

Learn how EtQ's Integrated FDA Compliance Management Software System:

  • guarantees compliance to regulations such as ISO 13485 and 21 CFR Part 11
  • addresss the needs of the Life Sciences industry, and exceed GMP standards
  • eMDR Submission Tool tool enables Medical Device Manufacturers to electronically submit MDRs to the FDA

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