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By working with Viedoc, we look forward to advancing clinical development in China and serving as a bridge between top modern EDC technology and innovative drug development.
Prof Yangfeng Wu, PUCRI
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Nordic CRO Larix signs Master Service Agreement with Viedoc

Nordic full-service CRO Larix has signed a master service agreement with Viedoc and will soon initiate the first clinical study powered by the Viedoc EDC system. “Viedoc’s big selling points are their streamlined setup process and a highly user-friendly interface. That’s exactly what our small- and middle-sized clients in the biotech industry are looking for in an EDC system,” says Lisa Thell, Director Data Management at Larix. Lisa Thell, Director Data Management at Larix. Larix works with several different EDC systems depending on the client and study at hand. “With

Functionality and Usability Reduce Lead Times – the Reason CRO Aptus Clinical Chose Viedoc

Functionality, API integration capabilities and overall usability were the key criteria when Clinical Contract Research Organization Aptus Clinical chose Viedoc as their new EDC system last year. “Viedoc was our first choice both when looking at the technical specification and more hands-on demonstrations. Now we can be completely self-sufficient in building our studies, which greatly reduces our lead times,” says Paul Blaney, Digital Health Lead at Aptus Clinical.With a 20-year track record of delivering Phase I-III clinical trials, Paul Blaney knows what it takes to be successful in

Trust, service and reliability – Here’s why Oslo University Hospital signed a 10-year EDC deal

For Oslo University Hospital it was a matter of trust, service and quality that helped them sign a 10-year deal with Viedoc . – We’ve been working with Viedoc for four years, and it was an obvious choice to extend our partnership. Auditing and evaluating a new EDC system is an extensive process, especially for us as a public institution. Now we know that we’ll have access to a high-quality EDC system that we’re used to working with for a long time to come, says Cecilie Moe, Manager Data

New partnership with Peking University – provides cloud-based EDC from within China

Viedoc today announced its partnership with Peking University Clinical Research Institute (PUCRI), a world-renowned academic center dedicated to enhancing the development of high-quality clinical research and health innovation in China. The partnership will accelerate the adoption of the Viedoc platform across the Chinese clinical research sector and, in doing so, help life sciences companies improve operational efficiencies and increase productivity across China's clinical research programs. Yvonne Zhou, MD Viedoc China, Prof Yangfeng Wu, Professor of Epidemiology at Peking

Oslo University Hospital signs 10-year enterprise deal with Viedoc

Collaboration to increase efficiencies in academic research across Norway Viedoc has signed a 10-year deal with Oslo University Hospital (OUH), the biggest contributor to medical and healthcare research conducted at Norwegian hospitals. The deal is an extension of Viedoc and OUH’s long-standing collaboration to help academic research improve operational efficiencies and increase productivity. "We are delighted to further strengthen our partnership with Viedoc. This extended partnership will provide better services and constitute an important tool for academic research in Norway", says

Correction of ePRO data

Should patients be able to change their submitted data? And if so, who is allowed to make changes, when can changes be made, and how will it affect the balance between data authenticity and data quality? Regulatory authorities recently issued a critical finding to a commercial ePRO vendor due to processes related to data integrity of ePRO data. One of the identified issues was that incorrect data submitted into the ePRO system could not be changed and were subsequently included in the study results. Requests to change the incorrect data had been submitted by the investigators but

LINK Medical – new partner with a three-year deal

Viedoc has initiated a partnership with European full-service contract research organization LINK Medical. To help accelerate clinical trials and optimize outcomes, LINK Medical has signed a three-year deal with Viedoc using Viedoc’s cloud-based EDC platform. Link Medical CEO Ola Gudmundsen, left, with Uwe Anzenberger, General Manager of Link Medical Germany. “As Master Viedoc users, we’re excited to formalize a partnership with Viedoc to secure the delivery of top-class EDC services for the coming three years. LINK Medical has extensive EDC expertise inhouse and it is

Blueclinical Expands Business with Viedoc to Accelerate Bioequivalence and Early-Stage Clinical Studies

Viedoc is expanding its partnership with Portuguese clinical research organization Blueclinical to help facilitate more efficient drug development. Blueclinical will increase its use of Viedoc as part of its service offering and will double the number of studies from current 15 to 30 performed with Viedoc. The contract period for the new deal is for three years. John Overend, Viedoc Sales and Marketing Manager “We’re excited to expand our partnership with Viedoc to support our clinical research. Blueclinical has used Viedoc for many years and together we will continue helping

Uppsala University Hospital facilitates patient studies with Viedoc

The Clinical Research and Development Unit at Uppsala University hospital has signed a three-year contract to use Viedoc as their primary EDC system. The hospital now has access to a world-class EDC and ePRO solution. The two parties will also be working together to further develop Viedoc in order to find improved ways to facilitate clinical research. “Viedoc provides Uppsala University Hospital with the resources to carry out more numerous and more effective clinical studies,” says Henrik Blombergsson, co-founder and COO of Viedoc. Henrik Blombergsson, co-founder and COO of

Viedoc and late phase studies – the perfect match

Late-phase studies are growing! And they are doing so by almost every metric: size, complexity, popularity, and simply the number of studies. However, they are not growing because they are easy to implement! Indeed, recruiting a representative sample for such studies typically globalizes the project, creating many challenges, such as navigating different languages, regulatory environments, social healthcare systems, third-party vendors, etc. Additionally, some investigators may have no prior experience in clinical research or the processes and technology involved. Thus, when preparing to

Improved site support by removing the help desk – a true Viedoc story

Should a centralized helpdesk provide tech support for studies all over the world, or should a small team from each study with full knowledge of the protocol solve technical issues directly? This was a major discussion point within the Viedoc team when we were redesigning the platform in early 2013. We found that a majority of the issues sent to the help desk tickets were minor technical issues, which took an unnecessarily long time for an unfamiliar technician to solve. A centralized help desk generally has non-specific knowledge about the study protocols, as well as no personal

Pfizer, China and 250 000 patients – the major Viedoc milestones during the first 15 years

Want to know what we have been doing for the last 15 years? Here are the milestones that reshaped the EDC-market with a straightforward software-as-a-service tool. 2003 It’s all about the looks The idea behind Viedoc was born in Uppsala, Sweden, by two former CRO-colleagues after winning a competition held by Sweden’s largest real estate company. The prize was a rental free office for 6 months which gave the business a kick-start. The business idea was to bring freshness to the outdated world of clinical data capture with a software that was not only nice to look at but also

It’s all talk. Here is how Viedoc walks GDPR

The buzzwords and GDPR strategies are flying around as enforcement day of May 25 is approaching. Here are the concrete steps we have taken to nail compliance with the new regulations. And by the way - our flexible platform made the work rather easy. 1. Encrypted data storage We have always encrypted all sending and receiving of data. But we felt that it was not enough. We have now chosen to encrypt the data at rest, when stored in our data centers. Why? GDPR is demanding “appropriate level of security” when it comes to transmitted, stored and processed data. Encryption of

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