Explore MACRO
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?
- Clinical researchers and trial coordinators seeking a dependable solution for data collection and management.
- Data managers and IT professionals requiring compliance-focused software tailored to clinical trial requirements.
- 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.
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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.
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MACRO Pricing
To cancel a MACRO product, check the specific cancellation policy of the vendor. Typically, orders can be cancelled within a certain timeframe, such as 48 hours. Contact customer service for assistance.
Most frequent question about MACRO
A MACRO product typically refers to a product or service that is designed to meet broad market needs, focusing on large-scale consumer appeal and societal impact.
A MACRO product targets a mass market, emphasizing societal and economic impacts, whereas a micro product focuses on individual needs and specific market segments.
Key strategies include using mass media advertising, optimizing product packaging, ensuring in-store availability, and leveraging social media platforms to reach a wider audience.
Social responsibility is crucial for MACRO products, as they often involve ethical considerations and environmental sustainability to appeal to a broader consumer base.
MACRO products influence consumer behavior by aligning with societal trends, such as environmental awareness, and by creating mass appeal through effective marketing strategies.
Try these alternatives of MACRO
Viedoc is a user-friendly and future-proof Electronic Data Capture (EDC) system designed to streamline clinical trials for pharmaceutical, biotech, and medical device industries. It offers intuitive tools for securely collecting, managing, analyzing, and validating trial data, enhancing efficiency and compliance. Trusted by organizations worldwide since 2003, Viedoc emphasizes flexibility, innovation, and a modern interface to empower clinical research teams.
REDCap is a secure web application designed for creating and managing customizable online surveys and databases. Tailored for research and operational use, it supports data capture in compliance with global regulations like HIPAA and GDPR. It offers features like branching logic, file uploads, automated data export, and audit trails for enhanced usability and security. REDCap is widely used by institutions worldwide, offering flexibility for both online and offline data collection.