MACRO:
Clinical Trial Management Software

One system for trial oversight, site management, and operational control.

MACRO EDC - The MACRO Advantage

MACRO EDC is valuable to customers because of the data integrity, data management and compliance features it provides. MACRO’s easy-to-use system allows users to quickly enter, track and report on subject data to collect accurate and reliable data for analysis.

Staff and software are audited in accordance with Good Clinical Practice (GCP) to demonstrate compliance with internationally-accepted ethical and scientific quality standards for designing, conducting, recording and reporting clinical trials involving human subjects. MACRO users can be assured that the rights, safety and health of their trial subjects will be protected, and the results of their clincial trials will be reliable and accurate.

MACRO is suitable for studies at all clinical trial phases, and is scalable for any size experiment. It can be used by small, medium or large organisations for single-site studies and multi-national trials.

MACRO Features

Compliance and Audit

Study Design

Data Input

Data Management

System Management and Security

Customer Support

Clinical

A Comprehensive Solution to Capture and Manage Clinical Trial Information

The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises.

Efficiently & Securely Capture & Manage Clinical Trial Information

The Ennov Clinical suite consists of Clinical Data Management applications (EDC, RTSM and ePRO) as well as Clinical Trial Management applications (CTMS and eTMF) that are available for deployment in the cloud or on premises.

Why Choose Ennov

Over 500,000 users trust Ennov

Providing you freedom of choice

Cloud-based or On Premises

Multi-Platform

ISO 9001 & 27001 Certified

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