Nordic CRO Larix signs Master Service Agreement with Viedoc
PRESS RELEASE / 2019-06-25
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.
Larix works with several different EDC systems depending on the client and study at hand.
“With Viedoc, we get an EDC system which allows our clients to focus entirely on their research, instead of spending large amounts of time on lengthy setup processes and learning how to manage the system. We want the best solution for every given study when offering an EDC solution to our clients.”
“We’re excited to start working with Larix and get the first study underway. Our goal from the start has been to make electronic data capture smarter, faster and easier than ever before – so it’s rewarding that Larix has chosen our system based on those exact factors,” says Henrik Blombergsson, COO and co-founder Viedoc.
Larix is a family founded, privately-owned CRO offering solutions in statistics, data management, clinical operations, medical writing, pharmacovigilance and data monitoring committees. Larix was founded in 2001 by Klaus Juel Olsen. In 2003, the company expanded with services within data management, and additional statisticians were employed. The clinical research service was added in 2008, simultaneously with an independent QA function. In 2010 the services were broadened to include pharmacovigilance. In 2015 Larix expanded to Sweden, Norway and Finland and as next step the Swedish office is now moving into Medicon Village in Lund. With more than 60 highly-qualified employees Larix has broad experience and therapeutic expertise in all aspects of clinical development in the biotechnology, medical device and pharmaceutical industries.
For more information, please contact:
New partnership with Peking University – provides cloud-based EDC from within China
PRESS RELEASE / 2019-04-23
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.
PUCRI has a wide range of partners within the clinical research sector, including government organizations, over 300 hospitals, hundreds of pharmaceutical companies and CROs across the country. As a result of PUCRI’s partnership with Viedoc, the university will be provided with cloud-based EDC technology, served from servers within China.
"We are delighted to initiate a partnership with Viedoc. Being able to store data within China is extremely important for Chinese domestic companies. 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", says Prof Yangfeng Wu at PUCRI.
Yvonne Zhou, Viedoc’s managing director China, says: "This is a collaboration that benefits all parties. Leveraging PUCRI's clinical trial expertise will enable us to serve more life sciences organizations in China and to accelerate drug development, allowing patients to access new therapies faster, both from the local market and around the world."
About Peking University Clinical Research Institute(PUCRI)
Peking University Clinical Research Institute (PUCRI) was founded in 2008, under the direct leadership of Peking University Health Science Center (PUHSC), as the first university-established public platform in China specialized in teaching, research, services, training, organizational coordination and technical support of clinical research. The institute also hosts the Peking University - APEC Regulatory Science Center of Excellence.
PUCRI is committed to improving clinical research in China, to promote the innovation in clinical medicine and hence people's well-being. PUCRI provides technical support to various clinical studies including new drug development, specifically research design, execution, quality management, data management and statistical analysis.
For more information, please contact any of the following:
Oslo University Hospital signs 10-year enterprise deal with Viedoc
PRESS RELEASE / 2019-03-06
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 will constitute an important tool for academic research in Norway", says Cecilie Moe, Manager Data Management Section, OUH.
The partnership deal spans over 10 years with an option to additional 5+5 years. The deal will secure OUH’s access to Viedoc’s EDC technology, which will be instrumental in optimizing local drug development programs by bringing operational efficiencies and greater speed to clinical trials.
John Overend, Viedoc’s Managing Director Sales and Marketing, "It is extremely satisfying to see that Viedoc is OUH’s top EDC choice not only today but also in 10 years’ time. It confirms that we have one of the world’s most modern EDC platforms”.
About Oslo University Hospital
Oslo University Hospital carry out advanced patient treatment, research and trial treatments, give advice and provide education on international levels. The hospital is Scandinavia’s largest and each year carry out more than 1.2 million patient treatments. Oslo University Hospital is responsible for approximately 50 percent of all medical and healthcare research conducted at Norwegian hospitals and is a significant role player within the education of a large variety of health care personnel.
For more information, please contact:
LINK Medical – new partner with a three-year deal
PRESS RELEASE / 2019-02-11
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.
“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 essential for us to collaborate with a product that helps us deliver more efficient and effective trials,” says Ola Gudmundsen, CEO of LINK Medical.
“LINK Medical is establishing itself as a leading Scandinavian CRO and we’re happy to deliver the technology needed to support them in this process”, says John Overend, Global Sales and Marketing Manager at Viedoc.
About LINK Medical
LINK Medical is a true full-service contract research organization (CRO) providing product development services for the pharmaceutical and medical device industries across Northern Europe. LINK Medical offers a well-integrated local presence in the Nordics and Germany. Reaching from early phase development to post-marketing, the company has over 170 employees providing expert guidance across every aspect of a project – all from one source. LINK Medicals promise is to improve and accelerate product development through transformative methods, active communication and optimal solutions. As a strategic partner, LINK Medical provides expert competence and technology to enable evidence-based decision-making that support the delivery of superior clinical outcomes.
For more information, please contact:
Blueclinical Expands Business with Viedoc to Accelerate Bioequivalence and Early-Stage Clinical Studies
PRESS RELEASE / 2019-02-05
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.
“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 sponsors to deliver more efficient and effective trials,” says Luis Almeida, CEO of Blueclinical.
“Blueclinical has been with us for more than five years and we are delighted to see that our long term strategy with our customers is appreciated and are of course happy that Blueclinical are increasing their business with us”, says Viedoc Sales and Marketing Manager, John Overend.
Blueclinical is a privately owned independent full-service CRO focused on bioequivalence and early-stage clinical studies in healthy subjects and patients, translational medicine consultancy and site management. Blueclinical’s own Clinical Pharmacology Unit is in Porto, Portugal. Their 61-bed clinical ward benefits from its hospital location for access to logistic services and emergency support.
For more information, please contact:
Uppsala University Hospital facilitates patient studies with Viedoc
PRESS RELEASE / 2018-12-18
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.
The R&D Unit at Uppsala University Hospital’s cancer clinic will now use Viedoc in all its clinical studies. The unit accounts for about half of all clinical trials performed at the hospital. Currently, nearly 200 studies are ongoing. One goal of the partnership with Viedoc is that every patient will be able to volunteer for a research study, if they wish to do so.
“A structured, organized partnership means that we reduce our costs for clinical studies. At the same time, we can contribute to technology development for clinical studies in the cancer field, which benefits both our own research groups and many others," says Peter Asplund, Department Manager and Deputy Chief Executive Officer, in a press release.
In addition to contracting a new high-profile client and enabling research, the partnership will give Viedoc important feedback.
“Even though our system is built primarily for end users – the individual examiner or researcher – our dialogue is usually carried out exclusively with the client, which can be anything from pharmaceuticals to biotech companies and CRO’s. Now we will get more feedback straight from the end users”, says Henrik Blombergsson, and continues:
“Uppsala University Hospital is at the forefront of several research fields and Viedoc’s ambition is to lead the development of Electronic Data Capturing, so this is a fitting partnership. We’re looking forward to initiate the project.”
For more information, please contact:
Viedoc PMS – new product!
The long-anticipated Post Marketing Surveillance (PMS) application, Viedoc PMS™, is finally here! Viedoc PMS was launched Dec 6th, primarily for our Japanese clients, as PMS-studies are conducted differently in Japan compared to the rest of the world. Viedoc PMS is built on the same, world-class platform as our standard Viedoc application, which has been proven by real-world use for the last 5 years in every study phase, therapeutic area, and study type. Viedoc PMS, however, comes with additional features specific to the Japanese PMS workflow, such as support for collecting data in booklets, allowing data to be collected during a specific time period rather than a specific visit date, and sending/receiving data back and forth between site and sponsor – known in Japan as the Kaifu function.
With the addition of Viedoc PMS to Viedoc’s product portfolio, we are now offering the most advanced EDC system in the Japanese market!
If you are interested in knowing more about this new product, contact us here.
Welcome to the User Group Meeting 21 Nov 2018 in Amsterdam
Join us in Amsterdam on 21 November for another rewarding and educational day where we will share our experiences and learn from each other.
All current customers are welcome to participate but also companies and organizations interested in networking, sharing experiences and learning more about Viedoc. This UGM will cover the latest Viedoc updates, the 2019/2020 roadmap as well as interesting use cases from some of our clients.
The meeting will be followed by some food and drinks starting at 17:00 at Level Eleven.
Registration is now open so make sure to secure your spot as it is a limited ticket event.
Meet us at DIA 2018 Global Annual Meeting, June 24th - 28th in Boston
As always it is great to be part of this annual meeting with thousands of innovators from around the world. Make sure to find us at booth number 2347 where our CEO Mats Klaar and co-founder Sverre Bengtsson will show you the world’s most sophisticated EDC & ePRO solution. We will have live demos to show everyone why our EDC is gaining so much market share lately. With 15 years in the industry Viedoc is now a solid choice for more and more Clinical research companies. Contact us to meet!
Meet us in Barcelona at Oursourcing in Clinical Trials Europe 2018
We will be present at the 8th Outsourcing in Clinical Trials in Barcelona. Meet us at booth #64 where our CEO Mats Klaar and co-founder Sverre Bengtsson will show you the world’s most sophisticated EDC & ePRO solution. See how Viedoc is designed to be as intuitive as possible, saving time and frustration from users at every level, allowing clinical trial organizations to have more focus on their own innovation and leadership.
This conference will focus on data and trial technology, as well as pressing partnership and outsourcing challenges and innovations in the industry. Given the latest hot topic of GDPR compliance, we are happy to walk you through all the things we have done to be fully compliant with not only GDPR but also FDA, ICH GCP, GAMP 5, HIPPA, CDISC.
We look forward to seeing you there! Contact us to meet!
Bigger, Stronger & Older!
This month we are celebrating 15 years of successful operation! Viedoc is now used in more than 70 countries around the world and more and more studies are started using the world’s # 1 EDC system. Join us in our successful journey by contacting one of our sale representatives today. After the initial demo and product overview you will get access to the platform to be able to evaluate hands-on how a modern EDC product feels.
Enjoy your trial!
Alan Yeomans holding two webinars on eCF Requirements
Our knowledgeable Quality Manager Alan Yeomans is once again invited by eClinical Forum to host a webinar to an audience around the world. The webinar is called Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements) and will be offered twice: March 27th and then again on April 17.
Alan has over 30 years in the industry and has been a speaker at many of the top industry events like eClinical Forum, DIA and CDISC around the world.
Alan has been at the company for 10 years and through the years he has been an essential contributor to the development of Viedoc. Lately, he has supported the Viedoc team on GDPR compliance. Viedoc customers can trust they are using a system that complies with all industry regulations allowing them to concentrate on what they do best!
Viedoc - Enjoy your trial!
Meet us at BIO-EUROPE SPRING March 12- 14, Amsterdam, The Netherlands
Come meet us in Amsterdam! We’ll be at this year’s Bio-EUROPE SPRING 12th Annual International Partnering Conference. This year’s focus will be innovation and global collaboration. With a presence in 72 countries, and being Industry innovators, it will be exceptionally great to be here and network with professionals from biotech, pharma and finance industries. Contact us to meet there!
2018 ACDM Annual Conference
Join us in Brussels, on the 13th of March
We will be in Brussels in March and are very much looking forward to meet professionals in clinical data management. As industry innovators, we look forward to the excellent speaker panel and inspiring industry talks showcasing innovative solutions to everyday challenges as well as new topics on the horizon. We also look forward to showing how Viedoc is the best EDC solution in the market and show our innovative and easy to use product is ahead of the game when it comes to the upcoming GDPR implementations.
Come see us at Booth #4! Contact us before the event to meet or set up a demo.
Viedoc 4.39 is now available and we are happy to say it’s a release where we combine support for improved patient compliance as well as efficiency workflows helping our users focus on what they are good at. In this release you will find the following:
Multiple reminders - This is a great supporting feature to improve patient compliance making sure no scheduled ViedocMe activity is forgotten. Unlimited reminders can be set to remind the subject before and or after the scheduled event.
Advanced event and activity scheduling – This is a very nice update with the benefit of easily setting up recurring events. Possibility to define scheduled events as reoccurring which will significantly reduce the effort when setting up events for subject diaries.
Repeating forms – This is also supporting the study designers when the same form is needed to be filled in multiple times.
Export and API using a specific Viedoc version data structure
Meet us in Orlando Florida at 9th Annual SCOPE Summit
We are looking forward to attending the 9th SCOPE Summit in Orlando Florida. The summit will offer many interesting discussions in all aspects of clinical trials. Specifically interesting for us will be the discussions about clinical data strategy and analytics. This event brings together over 1400 delegates from industry leading Biotech/CRO/Pharma organizations.
We are very much looking forward to our UGM in Tokyo this coming December 8th. This special event is the third consecutive Japanese Post-marketing surveillance (PMS) UGM. As with other UGM we value the insight gained from the knowledge shared from Pharma companies’ experience in conduction PMS studies for example how to handle the E2B format among many other things.
eClinical Forum Asia Pacific Workshop in Tokyo
We are attending the eClinical Forum Asia Pacific Workshop in Tokyo the 4th and 5th of December, 2017. Representatives from Azbil, Bristol Meyers Squibb, CSL Behring, ERT, Glaxo Smith Kline, ICON, Janssen Pharmaceutical, Medidata Solutions, Boehringer Ingelheim, Novartis, Oracle and IQVIA are attending to discuss possible solutions to industry issues such as Japanese experiences of eCOA, how to validate computer systems developed using agile methods, GDPR and the Japanese Act on Personal Information Privacy, shared audits, the use of EDC systems for PMS in Japan, new solutions for archiving, the use of blockchain in clinical research and for updates on the work being performed by the various eClinical Forum working groups.
Meet us at the DMB Data Management Biomedical conference
We look forward to the Annual DMB Conference taking place at the “Cité Universitaire Internationale” in Paris on Tuesday November 14th.
This event will bring about 200 clinical data managers from different industry sectors to discuss topics including Oncology Hybrid Study, EU General Data Protection Regulation, Use of Connected devices / Cloud / Artificial Intelligence in Clinical trials, eConsent, and Central Monitoring. A wide variety of companies like Sanofi, Lyon University Hospitals, RENAPE Cancer Network, and more will share their presentations for an anticipated inspiring and educational experience.
Contact us to meet in Paris! Our product specialist, Lorenza Capatini, and Co-founder and Sr. VP Strategic Relations, Sverre Bengtsson will be there to discuss everything from high-to-low tech needs. Reach out to us and learn why Viedoc continues to be highly appraised by data managers.
Join us at the User Group Meeting in Frankfurt
Register today for our European User Group meeting in Frankfurt on November 22.
The User Group Meeting is an excellent opportunity to meet with Viedoc representatives and interact with other users within the industry. Topics include presentations from experts in GDPR, industry insights, Data Integration/API and Viedoc’s latest development and ongoing projects.
Listen | Contribute | Learn | Network
Wednesday, November 22, 2017 from 10:00 AM to 7:00 PM CET
Frankfurt am Main 60329
Agenda 10.00-10.30 Registration and coffee 10.30-10.35 Welcome 10.35-10.45 Business update and latest news, PCG 10.45- 11.10 Release highlights last 12 months, PCG 11.10 - 11:30 Data Integration & API, use-case, PCG 11.30-12.00 Quality Assurance in Viedoc, PCG, Alan Yeomans 12.00-13.00 Lunch 13.00-14.00 Preparing for the EU GDPR in Clinical and Biomedical Research, Isabelle Abousahl 14.00-14.15 Viedoc roadmap, PCG 14.15-14.30 IWRS integration with Viedoc, Annemarie Wagemans, Danone 14.30-14.45 Standard forms - library: process and governance, Elsbeth Verdonk, Danone 14.45-15.00 ViedocMe use by parents in an infant trial, Hanneke Lankheet, Danone 15.00-15.30 Coffee break 15.30-16.00 CRF Library to Visualization - made easy by Viedoc API, Divya Suryanarayanan, Zifo 16.00-16.20 Challenges working with multiple parties (Sponsor, DM company, CRO), Johan Schilt, Unilever 16.20-16.50 Panel discussion (More details to come) 16.50-17.00 Summary 17.00-19.00 Reception
Due to the limited availability of seats, early registration is strongly recommended to ensure your participation. Please note that we reserve the right to limit the number of people from each company.
Don't hesitate to contact us if you have any questions about the event or how to register. Here is a link to the Roomers hotel where the Viedoc team will be staying at.
Meet us at BIO-Europe 2017
Meet us in Berlin for BIO-Europe 2017. It is the largest life science partnering conference in the industry with world-class workshops, panels and thousands of pre-scheduled one-to-one meetings. This is the 23rd annual international conference strategically hosted in Berlin as it is one of the leading life sciences and healthcare industries centres in the world.
The partnering one platform is now open. Contact Mr. Sverre Bengtsson, Co-founder and Sr VP Strategic Relations to learn more about Viedoc, the world's most sophisticated EDC & ePRO platform. With an increase in sales with more than 100% over the last two years, Viedoc is currently making a major impact on CROs and biotech companies all around the globe.
Take this opportunity to meet Sverre and find out how Viedoc can help your organization manage your trials in a more efficient, cost-effective and compliant way.
BYOD, App, Web-based Application?
Things to consider when collecting data from patients using ePRO
Patient self-reported data is playing a key part in efficacy, quality of life assessment and safety data collection in clinical trials. Bring Your Own Device, aka BYOD, enables a patient to capture such data on a device the patient is already familiar with, e.g. a smartphone, tablet or computer.
ViedocMe, our web-based ePRO solution, is an integrated part of our EDC platform Viedoc and allows patients to report clinical trial information directly from their mobile devices into the eCRFs available in Viedoc. Thanks to the integration, deploying a study diary and/or questionnaire in ViedocMe is not only more cost-effective than traditional ePRO trials, but can also be done in much less time.
ViedocMe builds on our vision of the future for how to handle patient reported data. For more information and a comparison between different solutions, see our white paper “The Future of ePro Platforms”, written in 2015 and still accurate.
We will be at NLS Days Sept. 12-14th!
Sverre Bengtsson, one of our co-founders will be part of the Super Session 5 on Sept. 14, from 8.00 – 9.15 followed by a Q&A. Topic: Preclinical and Clinical Methodological Advancements –Plenary Room – Main Hall
Many of the service providers in life science R&D have their own research. They provide much more than just an extra pair of hands and they spend high amounts on in house development of their services. With this super session, we will highlight their efforts and importance for the life science ecosystem where many of the companies are small and source for the latest technologies for their research and development.
Contact us to meet up, we look forward to another great NLS Days!
Join us in Orlando at the SCDM 2017 Annual Conference, September 24-27
This yearly event brings together the largest group of Clinical Data Managers in the world. We have been attending the SCDM conference for many years now, and we are proud to be part of it again. The program is full of exciting keynote speakers, workshops, and sessions. Especially interesting to us will be “eSource and the World of Opportunities” and “Emerging Trends in Clinical Data Capture and Clinical Research Technologies”. Look for booth # 708 and contact us to meet up: https://www.viedoc.com/contact-us/.
Win a 12-month Viedoc license!
We offer SCDM 2017 participants a chance to win a 12-month license. Below are several ways to enter the raffle:
Come meet us at booth #708 and leave your business card.
Share our social media posts and come to the booth to enter you name.
The winner will be announced after the event and they will be notified via email. After the awarded price is given, the user will have 6 months to start the license.
Restrictions of the 12-month licence are:
For phase I/II studies
Up to 10 sites
We look forward to being at SCDM and meeting our customers in the US!
Viedoc Release: Facilitating lab data entry and management
Version 4.36 out now!
The new Viedoc feature, reference data including the new data element range item, makes it easy to enter data shared by many subjects. By centrally managing the reference data for different data sources it is now possible to fill in the reference values once and these will be automatically populated to the subject forms. As lab data is linked to a data source it is also possible to assign the same data to multiple data sources, allowing the site to choose which reference data to be used for a specific subject visit
Why nominate for the Viedoc Most Valuable Professional Award?
The passion born from improving electronic data capture for clinical trials is still our greatest goal and this has made us a leading provider in the industry. This goal can only be accomplished by the communication and collaboration we have with our users. That is why we have now introduced the Viedoc Most Valuable Professional (Viedoc MVP) award. The Viedoc MVP is given for outstanding contributions within the Viedoc community and to acknowledge those who are willing to share their passion, technical expertise and real-world knowledge of Viedoc, electronic data capture or clinical trials. A Viedoc MVP is awarded for individual contributions and the nominees are selected exclusively by the PCG Solution’s management team based on a review of accomplishments and achievements.
This year, we have given our first Viedoc MVP award to Makoto Yokobori at the User Group Meeting held in Tokyo on 13 June. Mr Yokobori was the first user to get our back end set up training back in 2008. Since then, he has gained and shared in-depth knowledge from all aspects of conducting clinical trials using Viedoc. Mr Yokobori is a true ambassador for good clinical practice and includes this thinking in the study design and how systems can best be incorporated to support and raise the quality of the study. He is full of ideas and has a strong interest in improving and developing the industry, much like why Viedoc was born.
Our yearly Viedoc User Group Meeting (UGM) Japan took place earlier this week on June 13th. It was the 8th consecutive meeting and was held at the Tokyo International Forum. This year’s gathering was the biggest so far. These meetings have been an excellent opportunity to learn from our client’s experience with Viedoc. We hear what they like about it as well as what works and what doesn’t. The forum is a brilliant way get to know our clients. It is created to understand our customer needs better as well as to share information within the industry.
During the meeting, 3 of the largest CROs in Japan presented their proficiency with Viedoc. It was extremely gratifying to learn from their experience and it gave us incredible insight to keep improving our product even more and stay ahead as a world leading EDC provider.
The evening ended with a reception where we further enjoyed talking to our clients. We thank the participation of everyone that made this event a success, and we are already look forward to next year’s event.
Viedoc has the largest geographic reach in Japan. It has become essential to provide this positive platform and we plan to keep with the yearly tradition. While UGM started in Japan, we have had UGMs in other places. The next one will be in the Fall in Frankfurt Germany for our European customers. More information to come on that after the summer.
Meet us at DIA 2017 Global Annual Meeting in Chicago
Meet us in Chicago JUNE 19-21 and make sure you come by booth 635.
DIA 2017 is the largest multidisciplinary event that brings together a community of life sciences professionals at all levels and across all disciplines, all with a common goal to foster innovation that will lead to the development of safe and effective medical products and therapies to patients.
Win a 12-month Viedoc license!
We offer DIA participants a chance to win a 12-month license. Below are several ways to enter the raffle:
Come meet us at booth 635 and leave your business card.
Book a demo. When you pre-book a demo at our booth, you automatically get registered for a chance to win.
Share our social media posts and come to the booth to enter you name.
The winner will be announced after the event and they will be notified via email. After the awarded price is given, the user will have 6 months to start the license. Restrictions of the 12-month licence are:
For phase I/II studies
Up to 10 sites
We look forward to being there and meeting our customers in the US!
Viedoc Release: File upload in ViedocMe
Version 4.35 out now!
Our latest Viedoc release version 4.35 supports file upload in our ePro system ViedocMe. This enables subjects to take pictures directly from their phones. This update includes many more useful details like the print study workflow feature, and the ability to export to Excel/CSV as one row per item. There are many more details in the release notes and you can also review the release highlights video.
White Paper: Preparing for the EU GDPR in Clinical and Biomedical Research
On the 25th of May, 2018 the new European Union (EU) General Data Protection Regulation (GDPR) comes into effect. Everyone who does business within the EU must follow this new regulation. PCG Solutions is a European company, and is subject to GDPR.
GDPR requires companies to have control of their information management and its governance. In the Clinical Research sector this has long been vital for the success of clinical drug development, so it is not a pivotal change to how companies work. Instead companies need to ensure that their internal policies are aligned with the regulations defined in GDPR.
This white paper explains what GDPR is, the responsibilities and obligations it entails and how it affects you in your dealing with the EU and with PCG Solutions. PCG Solutions customers cover the entire range of companies from those active in the EU with natural persons based in the EU in their studies, to the opposite extreme where the only contact with the EU is PCG Solutions itself. This white paper covers all scenarios so that no matter what your connection to the EU is you can easily see how you are affected.
The latest release of Viedoc, version 4.34, supports file upload, which enables sites to manage all kinds of files together with the eCRF data, i.e. photos, documents, PDFs, images etc. Through standard data checks there is also a possibility to control size, uniqueness, name etc of each file uploaded. Contact us today for more information on how to manage the files in your study.
We will be present at the CDISC Europe Interchange in London, April 24-28. Join the companies, organisations and institutions already using Viedoc and contact us to discuss how also you can get started using the world’s most sophisticated EDC system.
The implementation of the WHO Drug Dictionaries in Viedoc was on March 8 validated and certified by the Uppsala Monitoring Centre, the global leader in pharmacovigilance. This means that all Viedoc customers using WHO-DD enable their pharmacovigilance to work more efficient by utilizing the global de-facto standard for coding drug names.
Working for a better world
Safer use of modern and traditional medicines is an ambitious goal for all of us. It depends on patients and health professionals, health ministries, regulators, and manufacturers working actively together. The priority is to identify when patients suffer any kind of harm from their therapy and to reduce the risk of this happening in the future. Uppsala Monitoring Centre is a major part of this global effort.
Viedoc Release: VAS up!?
Version 4.33 out now!
The Viedoc 4.33 release adds support for a Visual Analog Scale (VAS) in ViedocMe, enabling subjects to use the VAS scale to indicate and submit the intensity of perceived pain or disease symptoms. ViedocMe supports a 10 cm VAS on iPad Mini version 2-4 devices, and logs the device used by the subject when answering.
Viedoc continues to deliver top quality EDC services, resulting in a jump in sales by 68 percent in 2016 compared to the previous year. The main reasons behind the increased sales are larger projects and more new clients. Japan continues to be the top market for a fifth consecutive year. Also, the new system features introduced during the year were well-received by the users.
2017 has started in a very positive way with a couple of larger projects signed already.
Enjoy your trial!
Viedoc Release: Data import
Version 4.30 out now!
Viedoc Release 4.30 Data import - the latest feature update on the Viedoc platform making transfer of data from different sources to Viedoc easier than ever. External data is converted into CDISC ODM clinical data format using a data mapping file and pushed into Viedoc through the Viedoc API. Contact us for more info.
Proud to host the spring meeting of the e-Clinical Forum in Uppsala, Sweden May 17-19, 2016.
Meet us in Hamburg 18-19 November 2015
14th Annual PCT Partnerships in Clinical Trials
PCG participates with chairman and presenter in the one day seminar arranged in collaboration with the Section for Clinical Trials, a part of the Swedish Pharmaceutical Society, and Medical Products Agency.
The Swedish Academy of Pharmaceutical Sciences has collected a panel of international experts from the British (MHRA), Danish (DHMA), and Swedish (MPA) regulatory agencies as well as from industry, vendors and academia. They will present current thinking on the use of electronic systems for Data Capture (EDC), Case Report Forms (eCRF), Patient Reported Outcomes (ePRO), Trial Master Files (eTMF) and data from Electronic Health Records (EHRs), as well as inspection findings that can be attributed to the use of such systems. The use and pitfalls of electronic systems will be presented from the point of view of both pharmaceutical industry, CRO and clinical site.
PCG attends the partnering event Bio Europe Spring in Paris 9-11 March 2015. Contact our co-founder Sverre Bengtsson for a face-to-face meeting.
Welcome to another exciting Viedoc User Group Meeting in Tokyo, Japan
Welcome to another exciting Viedoc User Group meeting in Tokyo, Japan. Our representatives will demonstrate the latest updates on the Viedoc platform incl. Viedoc3, ViedocPMS, ViedocMe and Viedoc 4.
Date: June 9, 2015 Time: 13:00 - 17:00 followed by a 2 hour reception Location: Swedish Embassy Auditorium and Hall
We're delighted to be moving to new premises
February 27, Uppsala, Sweden
As the growth continues, PCG Solutions is pleased to announce the move to a new larger location to accommodate the expansion of the team in Sweden. The new address is Dragarbrunnsgatan 46, Uppsala. The move is in keeping with PCG’s continued progress to expand and improve its business and customer satisfaction. Look out for an invitation. This is worth celebrating.
Meet us in Shanghai, May 24-27, 2015
7th DIA China Annual Meeting. Are you interested in EDC? Viedoc 4 is the world's most sophisticated EDC & ePRO platform and has now reached China. Meet Hazel He, Key Account Managerat the annual meeting and let her inspire you for your next trial.
Receiving data from your patients just got better
Introducing the new ViedocMe app. Easier, smoother & better looking. The new ViedocMe app is finally here. Spoil your patients with an app that they can use on their own device. Save time and keep track of patient compliance by following the progress in Viedoc Clinic. And if that is not enough, the new ViedocMe app now also allows patients to type from right-to-left. Enjoy your trial!