MACRO is a cloud-based electronic data capture solution designed specifically for clinical research. It creates a strong synergy between clinical research and practice, driving a virtuous circle of continual improvement in best practice. Engineered to adhere to ethical and scientific quality standards, MACRO enables researchers to rapidly collect accurate and reliable data for robust analysis. Its intuitive design and customizable layout ensure that every step—from designing studies and creating electronic case report forms (eCRFs) to managing data and monitoring patient visitations—is streamlined for efficiency.

This innovative solution belongs to the Clinical Trial Management category, a field where precision, compliance, and data integrity are paramount. MACRO meets rigorous compliance standards such as GCP and 21 CFR, while also conforming to international information security norms. Its ISO 27001 certification and adherence to WCAG2-AA accessibility standards highlight its commitment to quality and inclusivity.

MACRO offers a range of practical features that simplify various aspects of clinical trials:

• Self-Service eCRF Creation: Easily design and customize forms tailored to study needs.
• Secure Data Management: Benefit from comprehensive audit trails, stringent user management, and secure data export in multiple formats for in-depth statistical analysis.
• Robust Compliance: Built to meet ethical and regulatory standards, ensuring data integrity and safeguarding patient information.
• Intuitive Interface: A user-focused design that minimizes complexity, reduces training time, and enhances productivity.

Why Use MACRO?

• Enhanced Research Efficiency: Automate routine tasks so your team can focus on core research and analysis.
• Scalable and Flexible: Suitable for both small research teams and large organizations managing multiple complex trials concurrently.
• Continual Improvement: Regularly updated to incorporate user feedback, ensuring it evolves with the ever-changing clinical landscape.
• Secure and Reliable: An emphasis on data security and regulatory compliance helps maintain the highest standards in clinical research.

Who is MACRO For?

1. Clinical researchers and trial coordinators seeking a dependable solution for data collection and management.
2. Data managers and IT professionals requiring compliance-focused software tailored to clinical trial requirements.
3. Pharmaceutical companies and academic institutions needing scalable systems for complex study designs.

Explore MACRO to streamline your clinical trial processes and enhance data quality. For exclusive deals, visit the MACRO deals page.

Consider These Alternatives:

• RedCap
• Viedoc

MACRO is the dependable choice for clinical trial management, offering a comprehensive and compliant platform that evolves with your needs, so you can focus on groundbreaking research and innovation.