About MedSurv
MedSurv is a clinical data management software from MedSurv that supports various medical research activities. It combines data capture, SAE management, and remote monitoring to provide an all-in-one system for researchers. Certified eCRF since 2006, MedSurv ensures validated processes for clinical studies, non-interventional studies, patient registry, and post-marketing observational studies. This platform also facilitates randomization and document upload, making it a comprehensive solution for clinical data management. Key capabilities: MedSurv-Portal Clinical studies Non-interventional studies (NIS) Patient registry Post-marketing observational studies Best for: researchers and clinical trial managers that need an integrated approach to clinical data collection and management.
MedSurv (EDC) by MedSurv GmbH is a web-based electronic data capture platform purpose-built for clinical trials, observational studies, registries, and large-scale data acquisition. The system emphasizes validated eCRF workflows, integrated ePRO/eDiary modules, SAE management, remote monitoring, and document uploads — effectively grouping data capture, trial management, and site communication into a single portal aimed at regulatory compliance and study transparency. The user interface is pragmatic and study-centric: administrators and data managers work from a browser console designed around study objects (subjects, visits, CRFs), while site users see streamlined data entry screens with clear status markers and inline validation prompts. The layout is functional rather than flashy, prioritizing quick access to patient status, open queries, and monitoring tasks. This reduces training time for site staff but means advanced admin panels can feel dense to new users. Functionality covers the full EDC lifecycle. MedSurv supports configurable eCRFs with conditional branching and real-time edit checks, patient questionnaires/ePRO, audit trails for compliance, query management, randomization/RTSM features, and document upload with patient allocation.
Pros & Cons
- +Strong project management and personal support.
- +Fast response times and efficient communication.
- +User-friendly interface and highly adaptable.
- +Reliable, competent partner with certified quality.
- +Uncomplicated, quick implementation of changes.
- −No specific mention of data security protocols.
- −Pricing information is not provided.
- −Doesn't detail specific statistical analysis tools.
- −Limited information on integration with other systems.
- −No mention of offline data collection capabilities.
Features
Key features
- eCRF/ePRO
- A validated online system for capturing clinical trial data and patient-reported outcomes.
- Customizable Randomization
- The software features a customizable algorithm to ensure a reliable ratio for patient randomization.
- (S)AE Management
- The system automatically processes and manages serious adverse events, streamlining the reporting process.
- ePRO/eDiary
- Enables direct patient collection of questionnaires and diaries, which improves data accuracy and efficiency.
- Clinical Trial Management
- Provides daily updates on study data, recruitment status, and remuneration for transparency.
- Compliance
- The system is built to track all changes with an Audit Trail to meet legal requirements and ensure data integrity.
Additional features
- eCRF / ePRO
- A validated online EDC system for data capture in various types of medical studies.
- Audit Trail
- Tracks all changes made to data according to legal requirements.
- Randomisation
- Uses a customizable algorithm to ensure a reliable ratio for patient allocation.
- (S)AE Management
- Automatically processes and manages serious adverse events.
- Monitoring
- Allows for virtual data checks, current patient and visit status tracking, and center management.
- Data Management
- Includes an additional validation process to ensure data quality.
- Query Management
- Facilitates direct communication within the portal to resolve data queries.
- ePRO/eDiary
- Allows for the direct collection of patient questionnaires and diaries.
- Document Upload
- Enables users to upload documents and allocate them to specific patients.
- Clinical Trial Management
- Provides daily updates on study data, remuneration, and recruitment status.
Pricing
Countries & Languages
Interface languages
Billing currencies
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About MedSurv
MedSurv is a clinical data management software from MedSurv that supports various medical research activities. It combines data capture, SAE management, and remote monitoring to provide an all-in-one system for researchers. Certified eCRF since 2006, MedSurv ensures validated processes for clinical studies, non-interventional studies, patient registry, and post-marketing observational studies. This platform also facilitates randomization and document upload, making it a comprehensive solution for clinical data management. Key capabilities: MedSurv-Portal Clinical studies Non-interventional studies (NIS) Patient registry Post-marketing observational studies Best for: researchers and clinical trial managers that need an integrated approach to clinical data collection and management.
MedSurv Details
MedSurv's In-App Market Place
Does MedSurv have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), AUD (A$), CAD (C$), JPY (¥), CNY (¥), INR (₹), BRL (R$), CHF (CHF), SEK (kr)
Pros & Cons
- Strong project management and personal support.
- Fast response times and efficient communication.
- User-friendly interface and highly adaptable.
- Reliable, competent partner with certified quality.
- Uncomplicated, quick implementation of changes.
- No specific mention of data security protocols.
- Pricing information is not provided.
- Doesn't detail specific statistical analysis tools.
- Limited information on integration with other systems.
- No mention of offline data collection capabilities.
MedSurv's Support Options
Email Address
medsurv.sales@cloud-related.deContact
061879059147MedSurv's Alternatives
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