Enzyme: An Overview

Enzyme is an advanced Quality Management System (QMS) tailored for medical device, digital health, and biopharma organizations. It is designed to streamline quality processes and ensure adherence to critical industry standards such as cGMP, QSR, and ISO. Enzyme encompasses all phases of the product development lifecycle, providing a comprehensive suite of tools to enhance document control, change management, training, risk assessment, audits, complaints handling, nonconformance management, and CAPA (Corrective and Preventive Actions).

Enzyme: Main Features

1. Document Control
2. Change Control
3. Training Management
4. Design Control
5. Risk Management
6. Supplier Management
7. Audit Management
8. Complaints Handling
9. Nonconformance Management
10. Corrective and Preventive Actions (CAPA)

Enzyme: User Guide

1. Schedule a demo to explore Enzyme's functionalities.
2. Complete the onboarding process to familiarize yourself with the platform.
3. Import existing data into Enzyme for seamless integration.
4. Integrate Enzyme with your preferred tools to facilitate data transfer.
5. Utilize core features like document control, change control, and training to manage quality processes effectively.
6. Leverage additional features such as design control, risk management, supplier management, audits, complaints handling, nonconformance management, and CAPA as needed.
7. Adapt the system to fit your organization's workflows for optimal usability.

Enzyme: Pricing

• For detailed pricing options, please visit Enzyme Pricing.

Enzyme: User Reviews

• "Enzyme has transformed our quality management processes, making compliance so much easier!" – A satisfied user from a biopharma company.
• "The intuitive interface and comprehensive features have significantly improved our document control." – Quality Manager at a medical device firm.