Grepsr by Grepsr
Grepsr is a managed data extraction and web scraping service, offering a 'data-as-a-service' model. Instead of selling software, Grepsr provides a team of expert data engineers who...
GoResearch, developed by 2KMM, is a fully validated, innovative internet platform dedicated to electronic data capture (EDC) for clinical projects. It provides a secure, web-based environment specifically engineered to meet the rigorous regulatory and operational requirements of clinical research. The platform supports the creation of electronic case report forms (eCRFs), patient randomization, data management, monitoring, and reporting. Its 'fully validated' status indicates it is designed and maintained under a quality management system to ensure reliability, data integrity, and compliance with standards like FDA 21 CFR Part 11, making it suitable for pivotal trials. This platform is intended for sponsors, contract research organizations (CROs), an...
This platform is intended for sponsors, contract research organizations (CROs), and academic research centers conducting clinical trials that require a validated EDC system. It is ideal for clinical data managers, biostatisticians, and project managers working on studies where regulatory acceptance and data auditability are paramount.
Our verdict is that GoResearch is a serious, validation-ready EDC platform for clinical research. Its emphasis on being fully validated from the outset is a significant strength, positioning it as a trustworthy choice for clinical trials where regulatory compliance cannot be compromised.
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This platform is intended for sponsors, contract research organizations (CROs), and academic research centers conducting clinical trials that require a validated EDC system. It is ideal for clinical data managers, biostatisticians, and project managers working on studies where regulatory acceptance and data auditability are paramount.
These are common features buyers compare in Electronic Data Capture Software. Product-specific availability should be confirmed with the vendor.
Maintain a chronological record of system changes including specific timestamps for accountability.
Centralized software for managing the workflows of one or more clinical trials.
Centralize the collection and tracking of Case Report Forms (CRFs) for research accuracy.
Efficiently gathering and moving data from various multiple systems into a target system.
Validate data sets to ensure precision and eliminate inconsistencies.
Collect documents and data using decentralized hardware like network scanners and MFDs.
Categorize and label documents with metadata to enable efficient search and retrieval.
Digitize physical paperwork into high-quality electronic formats for storage and retrieval.
Centralize the organization and distribution of templates and completed forms.
Electronically collect data from various sources outside a central office.
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