viedoc™

Viedoc is providing a system that combines user-friendliness, functionality, quality and cost in a competitive way supporting small biotech companies with limited activities and budgets to obtain access to a modern eCRF solution directly. The system is developed and supported by a great team - which is even more important for a successful project than the technology itself.Christian MeyerChief Medical Officer, CARDOZDenmark

Быстро, удобно, дружелюбный интерфейс.

"Fast, convenient, user-friendly interface."Alexey AnpilogovProject ManagerRussia

Viedoc is easy to navigate, helps to monitor very effectively with the reports in the same system. Also queries are easily to be followed, Investigator and staff overviews on access in the same system and the live support people are very adequate. A fantastic system that has all in ONE…Jitske BeukemaCRANetherlands

Viedoc is an extremely user friendly system. Even sites with minimal electronic data capture experience are able to use the system easily. The prototype database enables the CRA to trouble shoot issues with the site study staff and provide them solutions in a timely way. The customer service is exceptional and helpdesk is quick to respond and resolve any issues. Both the site staff and CRAs have enjoyed using this EDC.Karen A. ManneringCRAUS

As a Clinical Data Manager, I am looking for a system that is easy to learn, understand and use. In addition to this I want a system that is focused on collecting clinical data as easily and effectively and accurately as possible. Viedoc is just that system that offers it all. Features and functionalities in Viedoc are effective on highly complicated Oncology studies. The helpdesk is also very friendly and effective.Andries ClaassenCDMAustralia

弊社のプロジェクトでは、ViedocをEDCツールとしてだけではなく、最小化法を利用した割付システムとして採用しています。Viedocの割付プロセスは簡単で、実際に患者登 録が予想以上に早く進んでいます。

"Randomization in Viedoc is easy and patient enrollment is faster than expected."代表取締役社長　小田英世メディカル統計株式会社Japan

Viedoc is an easy to use, well-organized and fast web-based eCRF system that I would recommend to all. It is extremely malleable, and almost anything is possible. There are many ways in which it can increase the quality of your data, e.g. by using IWRS, remote monitoring, standard checks and reminders, lab data uploads, data reduction/calculations and alerts/info sent by email, text and/or web to any user (including the patient). It is the backbone of our studies, with all PI's, site personnel, labs & other vendors, CRAs & management team working with Viedoc in a pre-specified role-dependent manner. A true delight to work with both Viedoc and PCG!Jos BloemersDirector Scientific Operations, EB LybridoNetherlands

Easy to use system - no difficulties training sites or new site members. Not a complicated process to learn. Can easily see status of CRFs. Ability for sites to add comments in logistical spaces as well as for the CRA to add their own comments. Never any unusual errors. Quick system. Can look at problems on any smartphone to assist sites quickly. Helpdesk incredibly polite and helpful. Always willing to direct you if they can't assist.Michelle GillenCRAUS

Viedoc is an excellent example of an eCRF system which is well suited for phase I studies because of its user friendly interface.Bengt DahlströmCEO, CTC Clinical Trial ConsultantsSweden

Partnering with PCG and utilizing the Viedoc EDC system has allowed our company to provide fast and efficient data management services to our clients. The efficiency of Viedoc complemented our ability to meet end of study deadlines weeks in advance.Dan CavalliniTrial Care International, LLCUS

As a PM, I find Viedoc easily allows me to track CRA/Monitor site visits, review and sign visit reports, keep track of individual site and aggregate study subject enrollment, as well as the status of data entry for each subject at each site. The laboratory uploads are invaluable in helping identify and resolve issues along the "supplier" line from subject to laboratory to the Viedoc database. Most importantly, the PCG team are very responsive to making changes to improve functionality and accuracy and the Helpdesk folks could not be more supportive.Marilyn AgneyClinical Study ManagerUS