Enzyme QMS Frequently Asked Questions

Enzyme QMS Frequently Asked Questions. Enzyme is a QMS (Quality Management System) software that helps medical device, digital health, and biopharma companies streamline their quality processes and ensure compliance with industry standards such as cGMP, QSR, and ISO. It covers all stages of the product development lifecycle and offers a range of features to support document control, change control, training, risk management, audits, complaints, nonconformance, CAPA (Corrective and Preventive Actions), and more.

FAQ about Enzyme

What is Enzyme?

Enzyme is a robust QMS software designed for the medical device, digital health, and biopharma industries. It optimizes quality processes and ensures compliance with critical standards such as cGMP, QSR, and ISO, supporting every phase of the product development lifecycle.

How to use Enzyme?

To start using Enzyme, schedule a demo to explore its features. Once onboarded, you can import your existing data and integrate with your tools for seamless data transfer. Utilize the core features, including document control, change management, and training, to manage your quality processes efficiently. Adapt Enzyme's advanced features such as design control, risk management, supplier management, audits, complaints, nonconformance, and CAPA to suit your organizational needs. The platform is designed to be user-friendly and adaptable to your specific workflows.