About Viedoc
Viedoc is an eClinical software platform from Viedoc Technologies that delivers clinical trial solutions. It provides dependable eClinical solutions, on-demand expertise, and effortless integrations so that users can achieve accurate and cost-effective clinical trials. Viedoc’s adaptable platform supports various clinical trial processes and is consistently top-rated for its reliability and user-friendliness. The platform ensures accuracy, security, and regulatory compliance, which are essential in the clinical research field. Key capabilities: eClinical solutions On-demand expertise Effortless integrations Regulatory compliance User-friendly interface Best for: clinical researchers and trial managers that need efficient management of clinical trial data.
Viedoc is an eClinical software suite designed to streamline clinical trial data management. Trusted by organizations worldwide, it offers a user-friendly and efficient platform that simplifies the process of capturing accurate trial results. The software is highly regarded for its quick setup, comprehensive management tools, and continuous reliability. Viedoc is particularly beneficial for pharmaceutical, biotech, medical device companies, and research institutions conducting clinical trials, helping them achieve better results with less time and effort. The platform provides a seamless user experience with an intuitive interface, allowing study teams and participants to interact easily with its features. With its clean design and straightforward navigation, users can manage data capture, reporting, and logistics with ease. Viedoc is optimized for web-based access, ensuring compatibility across different devices and operating systems, such as Windows and Mac OS, and functions across all browsers. Its cross-platform support enhances its accessibility for users worldwide. Viedoc offers comprehensive features designed to meet the needs of clinical trials. At its core, the platform includes powerful electronic data capture (EDC) tools, providing reliable and accurate data collection.
Pros & Cons
- +Clients and sites find Viedoc user-friendly for clinical trials, including those with drugs, medical devices, and IVDs
- +Design team is dedicated to ease of use and adding useful features (e.g., form linking)
- +Strong collaboration and trust between the service and customers
- +Frequent updates with new, valuable features
- −SDV status could be integrated within the same form, not separately
- −AE-CM linking feature is missing
- −Managing roles and rights for specific designs is difficult
- −Lack of offline usability
- −No autopopulation for Conmeds from the WHO Drug dictionary
Features
Key features
- Electronic Data Capture (EDC)
- Viedoc’s core function is electronic data capture, which ensures accurate, reliable, and timely collection of clinical trial data. It eliminates manual processes, enhancing data integrity and reducing errors.
- Comprehensive Reporting
- Viedoc’s reporting tools allow users to create customizable reports for trial progress, performance, and safety data. The platform provides detailed insights into study metrics.
- Wearable Device Integration
- The platform supports wearable device data integration, allowing real-time data collection from devices like smartwatches. This feature ensures that data from remote monitoring is seamlessly captured.
- Regulatory Compliance
- Viedoc ensures full compliance with global regulatory standards like 21 CFR Part 11, ISO 27001, and HIPAA, safeguarding data security and maintaining trial integrity.
Additional features
- Study Setup & Management
- Centralized platform to manage all aspects of the trial process.
- Data Capture & Analytics
- Fast data collection and actionable insights through powerful analytics tools.
- Customizable Dashboards
- Tailored user dashboards to manage data visualizations and reporting.
- Real-Time Data Monitoring
- Provides access to trial data in real-time for better decision-making.
- Secure Signature Collection
- Digital signatures for document signing, ensuring compliance.
- Trial Closeout Tools
- Features to streamline the final stages of a trial, from data cleaning to final reporting.
Pricing
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Available in
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About Viedoc
Viedoc is an eClinical software platform from Viedoc Technologies that delivers clinical trial solutions. It provides dependable eClinical solutions, on-demand expertise, and effortless integrations so that users can achieve accurate and cost-effective clinical trials. Viedoc’s adaptable platform supports various clinical trial processes and is consistently top-rated for its reliability and user-friendliness. The platform ensures accuracy, security, and regulatory compliance, which are essential in the clinical research field. Key capabilities: eClinical solutions On-demand expertise Effortless integrations Regulatory compliance User-friendly interface Best for: clinical researchers and trial managers that need efficient management of clinical trial data.
Viedoc Details
Viedoc's In-App Market Place
Does Viedoc have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
NA
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (CHF), CNY (¥), SEK (kr), DKK (kr), NOK (kr), SGD (S$), HKD (HK$), KRW (₩), INR (₹), RUB (₽).
Pros & Cons
- Clients and sites find Viedoc user-friendly for clinical trials, including those with drugs, medical devices, and IVDs
- Design team is dedicated to ease of use and adding useful features (e.g., form linking)
- Strong collaboration and trust between the service and customers
- Frequent updates with new, valuable features
- SDV status could be integrated within the same form, not separately
- AE-CM linking feature is missing
- Managing roles and rights for specific designs is difficult
- Lack of offline usability
- No autopopulation for Conmeds from the WHO Drug dictionary
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