Enzyme QMS Introduction

Enzyme QMS Introduction. 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.

Enzyme Website screenshot

Understanding Enzyme

Enzyme is a comprehensive Quality Management System (QMS) software tailored for the medical device, digital health, and biopharma sectors. It facilitates streamlined quality processes and ensures adherence to industry standards such as cGMP, QSR, and ISO. Enzyme's features encompass the entire product development lifecycle, supporting functions like document control, change management, training, risk assessment, audits, handling complaints, managing nonconformances, and implementing CAPA (Corrective and Preventive Actions).

Getting Started with Enzyme

To begin using Enzyme, schedule a demo to familiarize yourself with its functionalities. Post onboarding, you can import existing data and integrate Enzyme with your current tools to enable smooth data transfer. Utilize core features like document control, change management, and training to efficiently oversee your quality processes. Additionally, Enzyme's design control, risk management, supplier management, audits, complaint handling, nonconformance management, and CAPA features can be tailored to meet your organization’s specific requirements. The platform is user-friendly and adaptable, fitting seamlessly into your workflow.