Viedoc shortens setup times while raising standards by introducing study templates

The life science industry has been challenged into rapidly changing how clinical trials are conducted. For Covid-19 studies, there has been a need to act more swiftly and set up databases faster than ever before. But the need for high-quality setups is still as high as ever before. After the pandemic, it will continue to be advantageous for companies to shorten setup times while maintaining quality in the race to return to normal. To ensure our clients can produce the highest quality setups while saving time, Viedoc is now introducing study templates.

Shorter setup times—today
Viedoc provides industry-leading setup times already today. Because Viedoc is a unified database, achieving rapid setup times is built into its DNA. All Viedoc's features and functionalities are accessible with a single login. The Designer and Admin tools are used for all configurations in Viedoc studies. The entire study design is also made in one application—no integrations, no delays, no hassle.

New studies in under four weeks
When designing a new study in Viedoc, the CRF library supplies users with a rich set of forms and associated edit checks. Using the provided CDISC CDASH forms, short-time study builds are the norm. Because Viedoc natively supports CDISC ODM files, you can:

• easily import a previous study design in the CDISC ODM format
• including all settings
• make the necessary changes
• and, most importantly, go live quickly

Because there is only one Designer tool for your configuration, tasks including any of the following are completed without complication: form creation, edit checks, configurable roles, workflow process, integrations, ePRO/eCOA, randomization, and supply management, medical coding, and more.

So, what's new?
Even the most experienced study designer can learn new tricks. From October, study designers using Viedoc will have access to three high-quality pre-designed studies made by our professional services team. These studies can be used in whole or in part. Included with these sample studies are eCRF form templates, validation documents, and more, all to get you started as quickly as possible. Those with less experience building studies will see industry best practices in use and learn from them. Experienced users can save time by "cherry-picking" the best bits and raise their quality standards to standards of excellence.

Enjoy your trial!