Six Reasons Why Viedoc is the
Right Fit for Clinical Research
February 2, 2024
by
Viedoc
Viedoc has been accelerating clinical trials since 2003. Today, it's one of the fastest-growing eClinical platforms for modern data collection in clinical studies, having been used in over 5,000 trials, across 30,000 sites, and with over 1 million patients. Their state-of-the-art applications include EDC, ePRO/eCOA, eCRF, Televisits, eTMF, and more.
Viedoc's commitment to making clinical trial data more accessible, adaptable, and secure has made them a trusted provider among leading sponsors, institutions, CROs, and medical device companies. With their powerful tools and streamlined interface, Viedoc provides reliable access to user-relevant information, enabling users to manage all aspects of their clinical study in one engaging solution. Whether it's a traditional multi-site study or a decentralized trial, Viedoc's flexible, future-proof, and secure eClinical solution offers the speed, reliability, and ease of use needed to drive life-changing research forward.
Viedoc scales for any phase in any trial–the system provides a modern, intuitive interface, is secure, and compliant. Your CROs and trial sites can get up and running with Viedoc in less than half the time it takes with other EDCs.
Here are six reasons why Viedoc is the right fit for sponsors.
Improved data quality
Viedoc Clinic can be configured to enforce data validation rules and checks, so you can ensure that the data entered into the system is accurate and complete. You can also set different permissions so that only certain roles have access to certain types of data and patient information.
Increased efficiency
The Viedoc system can streamline many tedious and time-consuming tasks associated with data management, such as data entry and report generation. With Viedoc Reports, you can download and generate detailed reports from the patient to site to the country level, saving you time and effort.
Better data organization
Viedoc TMF is used to organize and store data in a structured and easily searchable format, which can make it easier to find and analyze the data you need. The software sources the essential files in your studies, so you can more easily satisfy regulators and audits.
Viedoc TMF supports the global standard, DIAs Reference Model, that provides a standardized way to organize the documents under zones, sections, and artifacts. That way, you can find articles faster.
Enhanced collaboration
Viedoc is cloud based. This means you can access it online anywhere at any time. Since users have access whenever, wherever, and can share data with team members and collaborators, regardless of their location, they can strengthen and improve collaboration and communication.
Greater data security
Viedoc can be configured to protect data with security measures such as two-factor authentication and user access controls, which can help prevent unauthorized access to the data. As well, it is compliant with GDPR, HIPPA, APPI, and GB/T 35273-2020. Viedoc as a company also implements an ISMS and is certified according to ISO 27001.
Facilitation of regulatory compliance
The Viedoc solution meets the requirements of regulatory bodies, such as the FDA, and helps organizations stay compliant with relevant regulations. With Viedoc your files are always a few clicks away, saving you time when it comes to inspections.
Conclusion
Viedoc offers world-class professional services that will help you with any questions or concerns at every step of the way.
If you want to save time, effort, and costs, while boosting your security while centralizing your workflow, you can book a demo with the Viedoc team at www.viedoc.com.
Solutions overview
Viedoc is a state-of-the-art cloud-based software solution that offers a comprehensive suite of tools designed to streamline clinical trials. Viedoc provides a unified platform that includes EDC, ePRO/ECOA, eCRF, eTMF, and more, all accessible through a single sign-on (SSO).
With Viedoc, organizations can simplify their clinical trial management process and improve their data quality while also enhancing collaboration and data security. This unique solution provides a centralized platform that can be accessed from anywhere, making it the perfect choice for sponsors looking to optimize their clinical trial workflow.
About ViedocViedoc designs engaging software for the life science industry. By accelerating clinical trials on all levels, Viedoc’s solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide. Headquartered in Uppsala, Sweden, Viedoc also has offices in America, France, Japan, Vietnam, and China.
Since Viedoc’s inception in 2003, over 1 million patients in more than 75 countries have participated in studies powered by Viedoc. Discover more at www.viedoc.com
