ついにViedoc PMSがリリースされました！
12月6日にリリースされましたViedoc PMSは、世界各国で実施されているPMS調査の中でも、特に日本の製造販売後調査に特化した製品です。
Viedoc PMSは、標準的なViedocと同じ世界基準のプラットフォーム上に構築されています。このプラットフォームは世界中ですべてのフェーズ、治療領域、および試験の種類において過去５年間の実績があります。
我々の製品郡にViedoc PMSを追加することで、PCG Japanは日本国内でのあらゆる試験、研究、調査に対応できる日本市場で最も高度はEDCシステムを提供しています！
Viedoc PMSに関するお問い合わせは、コチラまでお問い合わせください。
2019年3月11日から15日に、 スウェーデン本社の品質管理責任者が来日し、PCG Solutions、PCG Japan、 Viedocに関するオーディットに対応いたします。
Auditでは下記を公開いたします。
オーディットは御社にお伺いすることもできますし、弊社のオフィスで実施することもできます。実施場所につきましては、下記についてご勘案ください。
弊社品質管理責任者によるオーディットをご希望の場合は、日時・場所を下記のEメールアドレスまでご連絡ください。
受付担当：角間
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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.
Listen | Contribute | Learn | Network
PCG and Kazushi Kamitani have decided to go separate ways. We are grateful for the work he has done for PCG and wish him good luck in his future career. Any questions can be directed to Thomas Kaponen, Representive Director PCG Japan.
この3月にファーマ・コンサルティング・グループは15周年を迎えました。
Viedocは現在、全世界70か国以上で使われており、より多くの研究で、この最高のEDCシステムが使われるようになっています。
弊社営業担当までご連絡いただければ、あなたも最高のEDCシステムユーザーの仲間入りです。
少しでもご興味をお持ちの方は、こちらからデモにお申込みください。
デモ・製品概要をご覧いただければ、現代のスマートなEDCシステムを肌で感じていただけることうけあいです。
弊社Quality Manager・Alan Yeomansがwebinar開催のため、eClinical Forumに参加します。
テーマは「規制臨床試験の電子データ要件(eCF Requirements)」について、2018年4月17日に開催予定です。
今回スピーカーを務めるAlan Yeomansは30年以上の業界経験があり、これまでeClinical Forum, DIA, CDISC等の名だたるイベントでもスピーカーを務めるなど、スピーカーとしての経験も非常に豊富です。
また、AlanはPCGに在籍しているこの10年間、Viedocの発展に尽力しており、直近では、ViedocチームをGDPRコンプライアンスの面から支えていました。こうしたサポートを背景に、Viedocユーザーの皆さんは、すべての業界規制を順守しているシステムを使っている、と安心してご自身のタスクに注力することができます。
Version4.39がリリースされました！
Viedoc4.39が現在お使いいただけます。ユーザーの皆さまそれぞれが担当業務によりリソースを割ける効率的なワークフローの実現と、患者コンプライアンスの改善のため、弊社サポートを結集しました。このリリースから新しく使える機能はこちらです。
2月12～15日にフロリダ州・オーランドで開催される第9回Annual SCOPE Summitでお会いしましょう！今回のイベントでは、業界をリードするバイオテクノロジー企業／CRO／製薬企業から1,400名以上の代表者をお招きして、治験における進歩とイノベーションにフォーカスした、とても興味深いアジェンダをご用意しています。
ご参加希望の方はこちらから
11月14日 火曜日にパリの「Cité Universitaire Internationale」で開催されるDMB会議の年次総会に参加します。
このイベントでは、さまざまな産業分野の約200人の臨床データ管理者が、腫瘍学のハイブリッド研究について、EUの一般データ保護規制に関して、又、臨床試験、eConsent 、Central Monitoringにおいて接続できるデバイス / クラウド / 人工知能の使用について議論します。 サノフィ、リヨン大学病院、RENAPEがんネットワークその他の幅広い企業が、プレゼンテーションを分かち合い、刺激的で教育的な体験が期待されています。
当社のLorenza Capatini（プロダクト・スペシャリスト）と、Sverre Bengtsson（共同設立者・副社長戦略的関係担当者）が、ハイテクからローテクのニーズに至るあらゆるご相談に応じます。Viedocがデータ管理者から引き続き高い評価を受けている理由をお解りいただけるでしょう。私たちに連絡をください。パリでお会いしましょう！
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
When
Wednesday, November 22, 2017 from 10:00 AM to 7:00 PM CET
Where
Roomers
Gutleutstraße 85
Frankfurt am Main 60329
Germany
Preliminary 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.
ベルリンで開催されるBIO-Europe 2017に参加します。これは業界最大のライフサイエンスパートナーシップカンファレンスで、ここでは世界クラスのワークショップ、パネル、数千の1対1のミーティングなどが予定されています。 この第23回年次国際会議は、世界の主要なライフサイエンスおよびヘルスケア産業の中心地である、そのベルリンで開催されます。
皆様の業務のパートナーとなるプラットフォーム。世界で最も洗練されたEDC＆ePROプラットフォームであるViedocの詳細については、Sverre Bengtsson、（共同設立者・副社長戦略的関係担当者）にお尋ねください。 Viedocは過去2年間で売上高が100％以上に増加し、世界中のCROやバイオテクノロジー企業に大きな影響を与えています。
Viedocによって貴社の治験をより効果的で費用対効果に優れた方法で管理できることを、Sverreが皆様に直接ご説明いたします。
ePROを使用して患者からデータを収集する際に考慮すべきこと。
患者自身が報告したデータは、臨床試験における有効性、QOL評価、安全性データの収集において重要な部分を担っています。 Bring Your Own Device。つまり、患者にスマートフォン、タブレット、またはコンピュータなどの普段から慣れ親しんでいる装置を利用してもらうことで、そのようなデータを収集できるようにします。
当社のWebベースePROソリューションであるViedocMeは、EDCプラットフォームViedocと統合されていて、患者はViedocで利用可能なeCRFに自身のモバイルデバイスから臨床試験情報を直接報告することができます。 この統合により、ViedocMeで患者日誌や質問に回答することで、従来のePROトライアルよりもコスト効率が良いだけでなく、ずっと短い時間で実行することができます。
ViedocMeは、患者の報告データをどのように扱うかについての、私たちの未来へのビジョンに基づいて設計されています。 詳細及び、異なるソリューション間の比較については、2015年に出した白書、「The Future of ePro Platforms」をご参照ください。
ViedocMeのより詳しいご説明はこちらからどうぞ。
2017年7月10日～14日の間、 スウェーデン本社の品質管理責任者が来日し、PCG Solutions、PCG Japan、 Viedocに関するオーディットに対応いたします。
Auditでは下記を公開いたします。
オーディットは御社にお伺いすることもできますし、弊社のオフィスで実施することもできます。実施場所につきましては、下記についてご勘案ください。
弊社品質管理責任者によるオーディットをご希望の場合は、日時・場所を下記のEメールアドレスまでご連絡ください。
受付担当：菅澤
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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
Session description
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!
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:
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:
We look forward to being at SCDM and meeting our customers in the US!
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
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.
Learn all about the award and how to get nominated in our Viedoc MVP page.
Bigger, Better, Stronger.
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 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:
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:
We look forward to being there and meeting our customers in the US!
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.
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.
Download White Paper: Preparing for the EU GDPR in Clinical and Biomedical Research
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.
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!
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.
Version 4.29 out now!
The new functionalities in this release are:
Viedoc is a Platinum Sponsor of the annual DMB conference and welcome you to join us in our booth. The main topics for the conference this year are "Clinical Data, Real Data, Open & Big Data".
The event will be located at the Maison Internationale (Cité Internationale), Paris.
Experience Viedoc at SCDM in San Diego, Sep 11-14, 2016.
Take the opportunity to meet with our industry experts as well as getting a live demo of Viedoc. You will find us in booth #602.
Welcome to Viedoc User Group meeting 2016 in Tokyo, Japan. Our representatives will demonstrate the latest updates on the Viedoc platform incl. Viedoc3, ViedocPMS, ViedocMe and Viedoc 4.
Date: Tuesday June 14th
Time: 13:00 – 17:00 followed by reception 17:00 – 19:00
Location: Alfred Nobel Auditorium at the Swedish Embassy
The event is free of charge. Please register via Enable JavaScript to view protected content. by Friday June 3rd.
Version 4.25 out now!
Don't loose any important data. Remind your subjects. Version 4.25 out now!
The new functionalities in this release are:
Version 4.24 out now!
The new functionalities in this release are:
Proud to host the spring meeting of the e-Clinical Forum in Uppsala, Sweden May 17-19, 2016.
14th Annual PCT Partnerships in Clinical Trials
PCG Solutions will be present at PCT in Hamburg 18-19 November 2015. This is a great opportunity to meet and listen to both present and potential clients. If you want to meet us there for a talk or have a demo, please contact Mats Klaar, Enable JavaScript to view protected content., or Henrik Blombergsson, Enable JavaScript to view protected content..
PCG will be present at the DMB annual conference in Paris, November 10. Get a chance to see the world’s most sophisticated EDC system in action.
Discover a new generation of EDC and ePRO. Meet and discuss your needs with co-founder Sverre Bengtsson. Book a private demo with Enable JavaScript to view protected content..
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.
Date: 2015-09-22
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. 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
The event is free of charge. Please send your application to Enable JavaScript to view protected content. not later than May 15.
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.
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 Manager at the annual meeting and let her inspire you for your next trial.
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!
